APA

Helbig K. L., Lauerer R. J., Bahr J. C., Souza I. A., Myers C. T., Uysal B., Schwarz N., Gandini M. A., Huang S., Keren B., Mignot C., Afenjar A., Billette de Villemeur T., Héron D., Nava C., Valence S., Buratti J., Fagerberg C. R., Soerensen K. P., Kibaek M., Kamsteeg E., Koolen D. A., Gunning B., Schelhaas H. J., Kruer M. C., Fox J., Bakhtiari S., Jarrar R., Padilla-Lopez S., Lindstrom K., Jin S. C., Zeng X., Bilguvar K., Papavasileiou A., Xing Q., Zhu C., Boysen K., Vairo F., Lanpher B. C., Klee E. W., Tillema J., Payne E. T., Cousin M. A., Kruisselbrink T. M., Wick M. J., Baker J., Haan E., Smith N., Sadeghpour A., Davis E. E., Katsanis N., Corbett M. A., MacLennan A. H., Gecz J., Biskup S., Goldmann E., Rodan L. H., Kichula E., Segal E., Jackson K. E., Asamoah A., Dimmock D., McCarrier J., Botto L. D., Filloux F., Tvrdik T., Cascino G. D., Klingerman S., Neumann C., Wang R., Jacobsen J. C., Nolan M. A., Snell R. G., Lehnert K., Sadleir L. G., Anderlid B., Kvarnung M., Guerrini R., Friez M. J., Lyons M. J., Leonhard J., Kringlen G., Casas K., El Achkar C. M., Smith L. A., Rotenberg A., Poduri A., Sanchis-Juan A., Carss K. J., Rankin J., Zeman A., Raymond F. L., Blyth M., Kerr B., Ruiz K., Urquhart J., Hughes I., Banka S., Hedrich U. B. S., Scheffer I. E., Helbig I., Zamponi G. W., Lerche H. & Mefford H. C. (20190514). De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. : American journal of human genetics.

Chicago

Helbig Katherine L, Lauerer Robert J, Bahr Jacqueline C, Souza Ivana A, Myers Candace T, Uysal Betül, Schwarz Niklas, Gandini Maria A, Huang Sun, Keren Boris, Mignot Cyril, Afenjar Alexandra, Billette de Villemeur Thierry, Héron Delphine, Nava Caroline, Valence Stéphanie, Buratti Julien, Fagerberg Christina R, Soerensen Kristina P, Kibaek Maria, Kamsteeg Erik-Jan, Koolen David A, Gunning Boudewijn, Schelhaas H Jurgen, Kruer Michael C, Fox Jordana, Bakhtiari Somayeh, Jarrar Randa, Padilla-Lopez Sergio, Lindstrom Kristin, Jin Sheng Chih, Zeng Xue, Bilguvar Kaya, Papavasileiou Antigone, Xing Qinghe, Zhu Changlian, Boysen Katja, Vairo Filippo, Lanpher Brendan C, Klee Eric W, Tillema Jan-Mendelt, Payne Eric T, Cousin Margot A, Kruisselbrink Teresa M, Wick Myra J, Baker Joshua, Haan Eric, Smith Nicholas, Sadeghpour Azita, Davis Erica E, Katsanis Nicholas, Corbett Mark A, MacLennan Alastair H, Gecz Jozef, Biskup Saskia, Goldmann Eva, Rodan Lance H, Kichula Elizabeth, Segal Eric, Jackson Kelly E, Asamoah Alexander, Dimmock David, McCarrier Julie, Botto Lorenzo D, Filloux Francis, Tvrdik Tatiana, Cascino Gregory D, Klingerman Sherry, Neumann Catherine, Wang Raymond, Jacobsen Jessie C, Nolan Melinda A, Snell Russell G, Lehnert Klaus, Sadleir Lynette G, Anderlid Britt-Marie, Kvarnung Malin, Guerrini Renzo, Friez Michael J, Lyons Michael J, Leonhard Jennifer, Kringlen Gabriel, Casas Kari, El Achkar Christelle M, Smith Lacey A, Rotenberg Alexander, Poduri Annapurna, Sanchis-Juan Alba, Carss Keren J, Rankin Julia, Zeman Adam, Raymond F Lucy, Blyth Moira, Kerr Bronwyn, Ruiz Karla, Urquhart Jill, Hughes Imelda, Banka Siddharth, Hedrich Ulrike B S, Scheffer Ingrid E, Helbig Ingo, Zamponi Gerald W, Lerche Holger and Mefford Heather C. 20190514. De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. : American journal of human genetics.

Harvard

Helbig K. L., Lauerer R. J., Bahr J. C., Souza I. A., Myers C. T., Uysal B., Schwarz N., Gandini M. A., Huang S., Keren B., Mignot C., Afenjar A., Billette de Villemeur T., Héron D., Nava C., Valence S., Buratti J., Fagerberg C. R., Soerensen K. P., Kibaek M., Kamsteeg E., Koolen D. A., Gunning B., Schelhaas H. J., Kruer M. C., Fox J., Bakhtiari S., Jarrar R., Padilla-Lopez S., Lindstrom K., Jin S. C., Zeng X., Bilguvar K., Papavasileiou A., Xing Q., Zhu C., Boysen K., Vairo F., Lanpher B. C., Klee E. W., Tillema J., Payne E. T., Cousin M. A., Kruisselbrink T. M., Wick M. J., Baker J., Haan E., Smith N., Sadeghpour A., Davis E. E., Katsanis N., Corbett M. A., MacLennan A. H., Gecz J., Biskup S., Goldmann E., Rodan L. H., Kichula E., Segal E., Jackson K. E., Asamoah A., Dimmock D., McCarrier J., Botto L. D., Filloux F., Tvrdik T., Cascino G. D., Klingerman S., Neumann C., Wang R., Jacobsen J. C., Nolan M. A., Snell R. G., Lehnert K., Sadleir L. G., Anderlid B., Kvarnung M., Guerrini R., Friez M. J., Lyons M. J., Leonhard J., Kringlen G., Casas K., El Achkar C. M., Smith L. A., Rotenberg A., Poduri A., Sanchis-Juan A., Carss K. J., Rankin J., Zeman A., Raymond F. L., Blyth M., Kerr B., Ruiz K., Urquhart J., Hughes I., Banka S., Hedrich U. B. S., Scheffer I. E., Helbig I., Zamponi G. W., Lerche H. and Mefford H. C. (20190514). De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. : American journal of human genetics.

MLA

Helbig Katherine L, Lauerer Robert J, Bahr Jacqueline C, Souza Ivana A, Myers Candace T, Uysal Betül, Schwarz Niklas, Gandini Maria A, Huang Sun, Keren Boris, Mignot Cyril, Afenjar Alexandra, Billette de Villemeur Thierry, Héron Delphine, Nava Caroline, Valence Stéphanie, Buratti Julien, Fagerberg Christina R, Soerensen Kristina P, Kibaek Maria, Kamsteeg Erik-Jan, Koolen David A, Gunning Boudewijn, Schelhaas H Jurgen, Kruer Michael C, Fox Jordana, Bakhtiari Somayeh, Jarrar Randa, Padilla-Lopez Sergio, Lindstrom Kristin, Jin Sheng Chih, Zeng Xue, Bilguvar Kaya, Papavasileiou Antigone, Xing Qinghe, Zhu Changlian, Boysen Katja, Vairo Filippo, Lanpher Brendan C, Klee Eric W, Tillema Jan-Mendelt, Payne Eric T, Cousin Margot A, Kruisselbrink Teresa M, Wick Myra J, Baker Joshua, Haan Eric, Smith Nicholas, Sadeghpour Azita, Davis Erica E, Katsanis Nicholas, Corbett Mark A, MacLennan Alastair H, Gecz Jozef, Biskup Saskia, Goldmann Eva, Rodan Lance H, Kichula Elizabeth, Segal Eric, Jackson Kelly E, Asamoah Alexander, Dimmock David, McCarrier Julie, Botto Lorenzo D, Filloux Francis, Tvrdik Tatiana, Cascino Gregory D, Klingerman Sherry, Neumann Catherine, Wang Raymond, Jacobsen Jessie C, Nolan Melinda A, Snell Russell G, Lehnert Klaus, Sadleir Lynette G, Anderlid Britt-Marie, Kvarnung Malin, Guerrini Renzo, Friez Michael J, Lyons Michael J, Leonhard Jennifer, Kringlen Gabriel, Casas Kari, El Achkar Christelle M, Smith Lacey A, Rotenberg Alexander, Poduri Annapurna, Sanchis-Juan Alba, Carss Keren J, Rankin Julia, Zeman Adam, Raymond F Lucy, Blyth Moira, Kerr Bronwyn, Ruiz Karla, Urquhart Jill, Hughes Imelda, Banka Siddharth, Hedrich Ulrike B S, Scheffer Ingrid E, Helbig Ingo, Zamponi Gerald W, Lerche Holger and Mefford Heather C. De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias. : American journal of human genetics. 20190514.