Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein
Usher综合征和Leber先天性黑蒙在分子水平上通过一种新型的中心体九蛋白样蛋白亚型相关联。
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddn312
van Wijk, Erwin; Kersten, Ferry F J; Kartono, Aileen; Mans, Dorus A; Brandwijk, Kim; Letteboer, Stef J F; Peters, Theo A; Märker, Tina; Yan, Xiumin; Cremers, Cor W R J; Cremers, Frans P M; Wolfrum, Uwe; Roepman, Ronald; Kremer, Hannie
