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contentType Journal Article|Research Support, Non-U.S. Gov't
issn 2045-2322
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publicationName Scientific Reports
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bibliographicCitation AlTalbishi A, Zelinger L, Zeitz C, Hendler K, Namburi P, Audo I, Sheffer R, Yahalom C, Khateb S, Banin E, Sharon D. TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations. Scientific Reports. 2019 Aug 19;9(1):12047. doi: 10.1038/s41598-019-46811-7.
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date 2019-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/31427709
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language English
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title TRPM1 Mutations are the Most Common Cause of Autosomal Recessive Congenital Stationary Night Blindness (CSNB) in the Palestinian and Israeli Populations
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Total number of triples: 39.