Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis (Q37618639)
Jump to navigation
Jump to search
scientific article published on 23 September 2011
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis |
scientific article published on 23 September 2011 |
Statements
1 reference
Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis (English)
1 reference
Hui Wang
1 reference
James R Lupski
1 reference
Richard A Gibbs
1 reference
Claire Patenia
1 reference
Ali A Al-Rajhi
1 reference
Ming Cao
1 reference
Zhe Li
1 reference
Xianfeng Chen
1 reference
Athurva Gore
1 reference
Emad B Abboud
1 reference
Richard A Lewis
1 reference
Graeme Mardon
1 reference
Kun Zhang
1 reference
Rui Chen
1 reference
23 September 2011
1 reference
1 reference
1 reference
1 reference
Identifiers
1 reference