Unexpected heterogeneity due to recessive and de novo dominant mutations of GJB2 in an Iranian family with nonsyndromic hearing loss: Implication for genetic counseling
Nejat Mahdieh, Atefeh Shirkavand, Marzieh Raeisi, Mohammad Taghi Akbari, Mustafa Tekin, Sirous ZeinaliVolume:
402
Year:
2010
Language:
english
Pages:
308
DOI:
10.1016/j.bbrc.2010.10.021
File:
PDF, 252 KB
english, 2010