论文信息 - A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). - 字舞流文

A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).

D. Kelsell | A. Markham | P. Van de Heyning | P. Willems | N. Lench | R. Mueller | G. Van Camp | R. Smith | I. Schatteman | H. Capon | R. Smith