BBS10 frameshift mutation in a Turkish girl with Bardet Biedl Syndrome.


SÖYLEMEZ M. A. , GEÇKİNLİ B. B. , DELİL K. , ARSLAN ATEŞ E., TÜRKYILMAZ A., AVŞAR M. , ...More

The European Society of Human Genetics, European Human Genetics Conference, 27 - 30 May 2017

  • Publication Type: Conference Paper