Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration is a paper indexed in ScholarIQ from OpenAlex.
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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration has 207 citations in the OpenAlex counts ScholarIQ stores.
When was Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration published?
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration has 2012 year in the ScholarIQ index.
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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration has closed oa status in the ScholarIQ index.
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