Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration (Q24624430)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration |
scientific article |
Statements
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration (English)
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September 2012
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44
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9
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1035-9
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