首页>Experimental Eye Research>A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family
A novel 7 bp deletion in PRPF31 associated with autosomal dominant retinitis pigmentosa with incomplete penetrance in an Indian family
作者单位：Department of Human Genetics, Guru Nanak Dev University, GT Road, Amritsar, Punjab, India[1]Central University of Punjab, Bathinda, India[2]Institute for Medical Genetics and Human Genetics, Charité-Universit?tsmedizin, Berlin, Germany[3]
换一批
