reference/26227554

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/26227554

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startingPage	3032
bibliographicCitation	Mackay DS, Ocaka LA, Borman AD, Sergouniotis PI, Henderson RH, Moradi P, Robson AG, Thompson DA, Webster AR, Moore AT. Screening of SPATA7 in patients with Leber congenital amaurosis and severe childhood-onset retinal dystrophy reveals disease-causing mutations. Invest Ophthalmol Vis Sci. 2011 May 09;52(6):3032–8. doi: 10.1167/iovs.10-7025. PMID: 21310915.
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date	2011-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21310915 https://doi.org/10.1167/iovs.10-7025
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Screening ofSPATA7in Patients with Leber Congenital Amaurosis and Severe Childhood-Onset Retinal Dystrophy Reveals Disease-Causing Mutations
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