reference/917463

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/917463

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	571
issn	1476-5438 1018-4813
issueIdentifier	8
pageRange	561-571
publicationName	European journal of human genetics : EJHG
startingPage	561
bibliographicCitation	Gerber S, Perrault I, Hanein S, Barbet F, Ducroq D, Ghazi I, Martin-Coignard D, Leowski C, Homfray T, Dufier J, Munnich A, Kaplan J, Rozet J. Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis. European Journal of Human Genetics. 2001 Aug 30;9(8):561–71. doi: 10.1038/sj.ejhg.5200689.
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date	2001-08-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/11528500 https://doi.org/10.1038/sj.ejhg.5200689
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis
discusses	http://id.nlm.nih.gov/mesh/M0017890 http://id.nlm.nih.gov/mesh/M0373003 http://id.nlm.nih.gov/mesh/M0005620
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Total number of triples: 50.