Characterization of a new full length TMPRSS3 isoform and identification of mutant alleles responsible for nonsyndromic recessive deafness in Newfoundland and Pakistan
对一种新的全长TMPRSS3亚型进行表征,并鉴定出导致纽芬兰和巴基斯坦非综合征性隐性耳聋的突变等位基因
期刊:BMC Medical Genetics
影响因子:
doi:10.1186/1471-2350-5-24
Ahmed, Zubair M; Li, Xiaoyan Cindy; Powell, Shontell D; Riazuddin, Saima; Young, Terry-Lynn; Ramzan, Khushnooda; Ahmad, Zahoor; Luscombe, Sandra; Dhillon, Kiran; MacLaren, Linda; Ploplis, Barbara; Shotland, Lawrence I; Ives, Elizabeth; Riazuddin, Sheikh; Friedman, Thomas B; Morell, Robert J; Wilcox, Edward R