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Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration
PaperCitations, authors & open-access status
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration is a paper indexed in ScholarIQ from OpenAlex. ScholarIQ records 207 citations, 2012 year and closed oa status.
207
Citations
2012
Year
closed
OA Status