Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B. (Q50429380)
Jump to navigation
Jump to search
scientific article published on 8 August 2012
Language | Label | Description | Also known as |
---|---|---|---|
English | Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B. |
scientific article published on 8 August 2012 |
Statements
Next-generation sequencing identifies a novel compound heterozygous mutation in MYO7A in a Chinese patient with Usher Syndrome 1B. (English)
1 reference
Yu Liang
1 reference
Xiaoming Wei
1 reference
Yan Sun
1 reference
Jiansheng Xie
1 reference
Quan Shi
1 reference
Ning Qu
1 reference
Guanghui Yang
1 reference
Jun Cai
1 reference
Yi Yang
1 reference
Wei Wang
1 reference
Xin Yi
1 reference
8 August 2012
1 reference
413
1 reference
23-24
1 reference
1866-1871
1 reference