Phenotypic variability in PRPH2 as demonstrated by a family with incomplete penetrance of autosomal dominant cone-rod dystrophy is a research paper published in Documenta Ophthalmologica (2023). On theSindex it has a DataRank of 0. It has been cited 14 times.
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NIH Clinical Center
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NIH Clinical Center
Grant: 5P30CA013696
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Grant: R24EY028758
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Grant: R24EY027285
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Foundation Fighting Blindness
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New York Stem Cell Foundation
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NEI NIH HHS
Grant: K08 EY000408
NCI NIH HHS
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NEI NIH HHS
Grant: P30 EY019007
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Grant: U01 EY034590
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NEI NIH HHS
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FWCI
1.34
Citation Percentile
0.8%
Citation Trend
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