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 PICO Portal 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 PICO Portal 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 PICO Portal 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 PICO Portal index.
What is the DOI of Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration?
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What is the PMID of Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degeneration?
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