论文信息 - Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment. - 字舞流文

Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.

S. Leal | C. Cremers | J. Veltman | H. Kremer | F. Cremers | L. Hoefsloot | S. Basit | W. Ahmad | P. Huygen | M. Schraders | G. Ali | M. Ansar | Kwanghyuk Lee | J. Oostrik | H. Kunst | R. Admiraal