APA
Akizu N., Cantagrel V., Zaki M. S., Al-Gazali L., Wang X., Rosti R. O., Dikoglu E., Gelot A. B., Rosti B., Vaux K. K., Scott E. M., Silhavy J. L., Schroth J., Copeland B., Schaffer A. E., Gordts P. L. S. M., Esko J. D., Buschman M. D., Field S. J., Napolitano G., Abdel-Salam G. M., Ozgul R. K., Sagıroglu M. S., Azam M., Ismail S., Aglan M., Selim L., Mahmoud I. G., Abdel-Hadi S., Badawy A. E., Sadek A. A., Mojahedi F., Kayserili H., Masri A., Bastaki L., Temtamy S., Müller U., Desguerre I., Casanova J., Dursun A., Gunel M., Gabriel S. B., de Lonlay P. & Gleeson J. G. (20150706). Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. : Nature genetics.
Chicago
Akizu Naiara, Cantagrel Vincent, Zaki Maha S, Al-Gazali Lihadh, Wang Xin, Rosti Rasim Ozgur, Dikoglu Esra, Gelot Antoinette Bernabe, Rosti Basak, Vaux Keith K, Scott Eric M, Silhavy Jennifer L, Schroth Jana, Copeland Brett, Schaffer Ashleigh E, Gordts Philip L S M, Esko Jeffrey D, Buschman Matthew D, Field Seth J, Napolitano Gennaro, Abdel-Salam Ghada M, Ozgul R Koksal, Sagıroglu Mahmut Samil, Azam Matloob, Ismail Samira, Aglan Mona, Selim Laila, Mahmoud Iman G, Abdel-Hadi Sawsan, Badawy Amera El, Sadek Abdelrahim A, Mojahedi Faezeh, Kayserili Hulya, Masri Amira, Bastaki Laila, Temtamy Samia, Müller Ulrich, Desguerre Isabelle, Casanova Jean-Laurent, Dursun Ali, Gunel Murat, Gabriel Stacey B, de Lonlay Pascale and Gleeson Joseph G. 20150706. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. : Nature genetics.
Harvard
Akizu N., Cantagrel V., Zaki M. S., Al-Gazali L., Wang X., Rosti R. O., Dikoglu E., Gelot A. B., Rosti B., Vaux K. K., Scott E. M., Silhavy J. L., Schroth J., Copeland B., Schaffer A. E., Gordts P. L. S. M., Esko J. D., Buschman M. D., Field S. J., Napolitano G., Abdel-Salam G. M., Ozgul R. K., Sagıroglu M. S., Azam M., Ismail S., Aglan M., Selim L., Mahmoud I. G., Abdel-Hadi S., Badawy A. E., Sadek A. A., Mojahedi F., Kayserili H., Masri A., Bastaki L., Temtamy S., Müller U., Desguerre I., Casanova J., Dursun A., Gunel M., Gabriel S. B., de Lonlay P. and Gleeson J. G. (20150706). Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. : Nature genetics.
MLA
Akizu Naiara, Cantagrel Vincent, Zaki Maha S, Al-Gazali Lihadh, Wang Xin, Rosti Rasim Ozgur, Dikoglu Esra, Gelot Antoinette Bernabe, Rosti Basak, Vaux Keith K, Scott Eric M, Silhavy Jennifer L, Schroth Jana, Copeland Brett, Schaffer Ashleigh E, Gordts Philip L S M, Esko Jeffrey D, Buschman Matthew D, Field Seth J, Napolitano Gennaro, Abdel-Salam Ghada M, Ozgul R Koksal, Sagıroglu Mahmut Samil, Azam Matloob, Ismail Samira, Aglan Mona, Selim Laila, Mahmoud Iman G, Abdel-Hadi Sawsan, Badawy Amera El, Sadek Abdelrahim A, Mojahedi Faezeh, Kayserili Hulya, Masri Amira, Bastaki Laila, Temtamy Samia, Müller Ulrich, Desguerre Isabelle, Casanova Jean-Laurent, Dursun Ali, Gunel Murat, Gabriel Stacey B, de Lonlay Pascale and Gleeson Joseph G. Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction. : Nature genetics. 20150706.