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: elif uzay, Ayça AYKUT, Asude DURMAZ, Tahir ATİK, SARENUR GÖKBEN, Feriştah Ferda ÖZKINAY, Muhsin Özgür ÇOĞULU

13th Balkan Genetic Congress, International, Verbal, Full Text, 2019-2019

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