APA
Wortmann S. B., Ziętkiewicz S., Kousi M., Szklarczyk R., Haack T. B., Gersting S. W., Muntau A. C., Rakovic A., Renkema G. H., Rodenburg R. J., Strom T. M., Meitinger T., Rubio-Gozalbo M. E., Chrusciel E., Distelmaier F., Golzio C., Jansen J. H., van Karnebeek C., Lillquist Y., Lücke T., Õunap K., Zordania R., Yaplito-Lee J., van Bokhoven H., Spelbrink J. N., Vaz F. M., Pras-Raves M., Ploski R., Pronicka E., Klein C., Willemsen M. A. A. P., de Brouwer A. P. M., Prokisch H., Katsanis N. & Wevers R. A. (20150409). CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. : American journal of human genetics.
Chicago
Wortmann Saskia B, Ziętkiewicz Szymon, Kousi Maria, Szklarczyk Radek, Haack Tobias B, Gersting Søren W, Muntau Ania C, Rakovic Aleksandar, Renkema G Herma, Rodenburg Richard J, Strom Tim M, Meitinger Thomas, Rubio-Gozalbo M Estela, Chrusciel Elzbieta, Distelmaier Felix, Golzio Christelle, Jansen Joop H, van Karnebeek Clara, Lillquist Yolanda, Lücke Thomas, Õunap Katrin, Zordania Riina, Yaplito-Lee Joy, van Bokhoven Hans, Spelbrink Johannes N, Vaz Frédéric M, Pras-Raves Mia, Ploski Rafal, Pronicka Ewa, Klein Christine, Willemsen Michel A A P, de Brouwer Arjan P M, Prokisch Holger, Katsanis Nicholas and Wevers Ron A. 20150409. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. : American journal of human genetics.
Harvard
Wortmann S. B., Ziętkiewicz S., Kousi M., Szklarczyk R., Haack T. B., Gersting S. W., Muntau A. C., Rakovic A., Renkema G. H., Rodenburg R. J., Strom T. M., Meitinger T., Rubio-Gozalbo M. E., Chrusciel E., Distelmaier F., Golzio C., Jansen J. H., van Karnebeek C., Lillquist Y., Lücke T., Õunap K., Zordania R., Yaplito-Lee J., van Bokhoven H., Spelbrink J. N., Vaz F. M., Pras-Raves M., Ploski R., Pronicka E., Klein C., Willemsen M. A. A. P., de Brouwer A. P. M., Prokisch H., Katsanis N. and Wevers R. A. (20150409). CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. : American journal of human genetics.
MLA
Wortmann Saskia B, Ziętkiewicz Szymon, Kousi Maria, Szklarczyk Radek, Haack Tobias B, Gersting Søren W, Muntau Ania C, Rakovic Aleksandar, Renkema G Herma, Rodenburg Richard J, Strom Tim M, Meitinger Thomas, Rubio-Gozalbo M Estela, Chrusciel Elzbieta, Distelmaier Felix, Golzio Christelle, Jansen Joop H, van Karnebeek Clara, Lillquist Yolanda, Lücke Thomas, Õunap Katrin, Zordania Riina, Yaplito-Lee Joy, van Bokhoven Hans, Spelbrink Johannes N, Vaz Frédéric M, Pras-Raves Mia, Ploski Rafal, Pronicka Ewa, Klein Christine, Willemsen Michel A A P, de Brouwer Arjan P M, Prokisch Holger, Katsanis Nicholas and Wevers Ron A. CLPB mutations cause 3-methylglutaconic aciduria, progressive brain atrophy, intellectual disability, congenital neutropenia, cataracts, movement disorder. : American journal of human genetics. 20150409.