reference/7358189

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7358189

Outgoing Links

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endingPage	242
issn	1460-2083 0964-6906
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publicationName	Human Molecular Genetics
startingPage	230
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bibliographicCitation	Bujakowska KM, Zhang Q, Siemiatkowska AM, Liu Q, Place E, Falk MJ, Consugar M, Lancelot ME, Antonio A, Lonjou C, Carpentier W, Mohand-Saïd S, den Hollander AI, Cremers FP, Leroy BP, Gai X, Sahel JA, van den Born LI, Collin RW, Zeitz C, Audo I, Pierce EA. Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndrome. Hum Mol Genet. 2015 Jan 01;24(1):230–42. PMID: 25168386; PMCID: PMC4326328.
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date	2014-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome
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Total number of triples: 89.