A Novel HNF1B mutation in a family with two MODY patients


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

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

  • Publication Type: Conference Paper