Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B
Xiaoming Wei, Yan Sun, Jiansheng Xie, Quan Shi, Ning Qu, Guanghui Yang, Jun Cai, Yi Yang, Yu Liang, Wei Wang, Xin YiVolume:
413
Year:
2012
Language:
english
Pages:
1
DOI:
10.1016/j.cca.2012.07.022
File:
PDF, 1.80 MB
english, 2012