reference/26693970

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26693970

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endingPage	305
issn	1460-2083
issueIdentifier	2
pageRange	299-305
publicationName	Human Molecular Genetics
startingPage	299
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bibliographicCitation	Swaroop A, Wang QL, Wu W, Cook J, Coats C, Xu S, Chen S, Zack DJ, Sieving PA. Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function. Hum Mol Genet. 1999 Feb;8(2):299–305. doi: 10.1093/hmg/8.2.299. PMID: 9931337.
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date	1999-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/8.2.299 https://pubmed.ncbi.nlm.nih.gov/9931337
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Leber congenital amaurosis caused by a homozygous mutation (R90W) in the homeodomain of the retinal transcription factor CRX: direct evidence for the involvement of CRX in the development of photoreceptor function
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