A mutation in ATP11A causes autosomal-dominant auditory neuropathy type 2
ATP11A 突变导致 2 型常染色体显性听觉神经病
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddac267
Shashank Chepurwar, Sarah M von Loh, Daniela C Wigger, Jakob Neef, Peter Frommolt, Dirk Beutner, Ruth Lang-Roth, Christian Kubisch, Nicola Strenzke, Alexander E Volk
