Reverse phenotyping revealing rare ADAM22 gene mutation detected by whole exome sequencing in 2 early infantile epileptic encephalopathy siblings.

Conference paper > Full Text · 2019

Authors: Muhsin Özgür ÇOĞULU

13th Balkan Congress of Human Genetics, Turkey, Edirne, International, Invitee, Full Text, 2019-, pp 10-10

View details