Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family

por Park, Gibeom, Gim, Jungsoo, Kim, Arheum, Han, Kyu-Hee, Kim, Hyo-Sang, Oh, Seung-Ha, Park, Taesung, Park, Woong-Yang, Choi, ByungYoon
Publicado 2013