Whole-exome sequencing identifies ALMS1, IQCB1, CNGA3, and MYO7A mutations in patients with Leber congenital amaurosis
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| Description | scientific article published on 23 September 2011 |
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author: Hui Wang Claire Patenia Ali A Al-Rajhi Richard A Gibbs James R. Lupski Xia Wang Donna Muzny |
| Publication date | September 23, 2011 |
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