Exome sequencing identifies NMNAT1 mutations as a cause of Leber congenital amaurosis
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| Description | scientific article published on July 29, 2012 |
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author: Juliana M F Sallum Elise Héon Pei-Kuan Cong Richard G Weleber |
| Publication date | September 2012 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |