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
  • Marmara University Affiliated: Yes