论文信息 - A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies - 字舞流文

A heterozygous mutation in GJB2 (Cx26F142L) associated with deafness and recurrent skin rashes results in connexin assembly deficiencies

Patricia E. Martin | M. Zamiri | A. Waters | Ahmad Albuloushi | M. Lovgren | A. Steel | Yeelon Yeoh | P. Martin