A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family
暂无分享,去创建一个
S. Leal | K. Esoh | A. Wonkam | I. Schrauwen | Edmond Wonkam-Tingang | A. Nasir | T. Bharadwaj | Anushree Acharya | Liz M. Nouel-Saied | Thashi Bharadwaj