A novel HNF1B mutation in a family with two MODY patients


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

The European Society of Human Genetics 2017., KOPENHAGEN, Denmark, 25 - 28 May 2017

  • Publication Type: Conference Paper / Summary Text
  • City: KOPENHAGEN
  • Country: Denmark