Whole-exome sequencing identifies USH2A mutations in a pseudo-dominant Usher syndrome family

Author:        

Publisher: Spandidos Publications

E-ISSN: 1791-244X|36|4|1035-1041

ISSN: 1107-3756

Source: International Journal of Molecular Medicine, Vol.36, Iss.4, 2015-01, pp. : 1035-1041

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract