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


ÇOĞULU M. Ö.

13th Balkan Congress of Human Genetics, Edirne, Turkey, 17 April 2019, pp.10

  • Publication Type: Conference Paper / Full Text
  • City: Edirne
  • Country: Turkey
  • Page Numbers: pp.10