MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease

MLA

Janine Altmüller, et al. “MFSD2A-Associated Primary Microcephaly - Expanding the Clinical and Mutational Spectrum of This Ultra-Rare Disease.” European Journal of Medical Genetics, vol. 64, no. 10, Oct. 2020. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....376402307641ec337bbaf705064ae666&authtype=sso&custid=ns315887.

APA

Janine Altmüller, Nursel Elcioglu, Angela Köninger, Bernd Wollnik, Adela Della Marina, Frank J. Kaiser, Burcu Yeter, Gökhan Yigit, Carolina Martínez Grijalva, Anja Stein, Christel Depienne, Ute Hehr, Holger Thiele, Peter Nürnberg, Katharina Khuller, & Alma Kuechler. (2020). MFSD2A-associated primary microcephaly - Expanding the clinical and mutational spectrum of this ultra-rare disease. European Journal of Medical Genetics, 64(10).

Chicago

Janine Altmüller, Nursel Elcioglu, Angela Köninger, Bernd Wollnik, Adela Della Marina, Frank J. Kaiser, Burcu Yeter, et al. 2020. “MFSD2A-Associated Primary Microcephaly - Expanding the Clinical and Mutational Spectrum of This Ultra-Rare Disease.” European Journal of Medical Genetics 64 (10). http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edsair&AN=edsair.doi.dedup.....376402307641ec337bbaf705064ae666&authtype=sso&custid=ns315887.