APA
Assoum M., Philippe C., Isidor B., Perrin L., Makrythanasis P., Sondheimer N., Paris C., Douglas J., Lesca G., Antonarakis S., Hamamy H., Jouan T., Duffourd Y., Auvin S., Saunier A., Begtrup A., Nowak C., Chatron N., Ville D., Mireskandari K., Milani P., Jonveaux P., Lemeur G., Milh M., Amamoto M., Kato M., Nakashima M., Miyake N., Matsumoto N., Masri A., Thauvin-Robinet C., Rivière J., Faivre L. & Thevenon J. (20170523). Autosomal-Recessive Mutations in AP3B2, Adaptor-Related Protein Complex 3 Beta 2 Subunit, Cause an Early-Onset Epileptic Encephalopathy with Optic Atrophy. : American journal of human genetics.
Chicago
Assoum Mirna, Philippe Christophe, Isidor Bertrand, Perrin Laurence, Makrythanasis Periklis, Sondheimer Neal, Paris Caroline, Douglas Jessica, Lesca Gaetan, Antonarakis Stylianos, Hamamy Hanan, Jouan Thibaud, Duffourd Yannis, Auvin Stéphane, Saunier Aline, Begtrup Amber, Nowak Catherine, Chatron Nicolas, Ville Dorothée, Mireskandari Kamiar, Milani Paolo, Jonveaux Philippe, Lemeur Guylène, Milh Mathieu, Amamoto Masano, Kato Mitsuhiro, Nakashima Mitsuko, Miyake Noriko, Matsumoto Naomichi, Masri Amira, Thauvin-Robinet Christel, Rivière Jean-Baptiste, Faivre Laurence and Thevenon Julien. 20170523. Autosomal-Recessive Mutations in AP3B2, Adaptor-Related Protein Complex 3 Beta 2 Subunit, Cause an Early-Onset Epileptic Encephalopathy with Optic Atrophy. : American journal of human genetics.
Harvard
Assoum M., Philippe C., Isidor B., Perrin L., Makrythanasis P., Sondheimer N., Paris C., Douglas J., Lesca G., Antonarakis S., Hamamy H., Jouan T., Duffourd Y., Auvin S., Saunier A., Begtrup A., Nowak C., Chatron N., Ville D., Mireskandari K., Milani P., Jonveaux P., Lemeur G., Milh M., Amamoto M., Kato M., Nakashima M., Miyake N., Matsumoto N., Masri A., Thauvin-Robinet C., Rivière J., Faivre L. and Thevenon J. (20170523). Autosomal-Recessive Mutations in AP3B2, Adaptor-Related Protein Complex 3 Beta 2 Subunit, Cause an Early-Onset Epileptic Encephalopathy with Optic Atrophy. : American journal of human genetics.
MLA
Assoum Mirna, Philippe Christophe, Isidor Bertrand, Perrin Laurence, Makrythanasis Periklis, Sondheimer Neal, Paris Caroline, Douglas Jessica, Lesca Gaetan, Antonarakis Stylianos, Hamamy Hanan, Jouan Thibaud, Duffourd Yannis, Auvin Stéphane, Saunier Aline, Begtrup Amber, Nowak Catherine, Chatron Nicolas, Ville Dorothée, Mireskandari Kamiar, Milani Paolo, Jonveaux Philippe, Lemeur Guylène, Milh Mathieu, Amamoto Masano, Kato Mitsuhiro, Nakashima Mitsuko, Miyake Noriko, Matsumoto Naomichi, Masri Amira, Thauvin-Robinet Christel, Rivière Jean-Baptiste, Faivre Laurence and Thevenon Julien. Autosomal-Recessive Mutations in AP3B2, Adaptor-Related Protein Complex 3 Beta 2 Subunit, Cause an Early-Onset Epileptic Encephalopathy with Optic Atrophy. : American journal of human genetics. 20170523.