Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3.
与 Meckel 综合征基因 MKS1 和 MKS3 的突变和缺失相关的纤毛和中心体缺陷
期刊:Human Molecular Genetics
影响因子:3.2
doi:10.1093/hmg/ddp272
Tammachote Rachaneekorn, Hommerding Cynthia J, Sinders Rachel M, Miller Caroline A, Czarnecki Peter G, Leightner Amanda C, Salisbury Jeffrey L, Ward Christopher J, Torres Vicente E, Gattone Vincent H 2nd, Harris Peter C
