A founder mutation uncovers MPZL2 (DFNB111) as a novel autosomal recessive non-syndromic moderate hearing loss gene

barbara v., Bademci G., Abad C., İNCESULU Ş. A., rad a., ALPER Ö., ...Daha Fazla

German Society of Human Genetics Meeting, 6 - 08 Nisan 2019

  • Yayın Türü: Bildiri
  • Ankara Üniversitesi Adresli: Evet