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Case Reports|Letter|Research Support, Non-U.S. Gov't |
endingPage |
199 |
issn |
1442-9071 1442-6404 |
issueIdentifier |
3 |
pageRange |
197-199 |
publicationName |
Clinical & Experimental Ophthalmology |
startingPage |
197 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/organization/MD5_487baf6554eb36bb22c6138d90a7c50f |
bibliographicCitation |
Yang J, Huang XF, Tong Y, Jin ZB. Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome. Clin Exp Ophthalmol. 2016 Apr;44(3):197–9. doi: 10.1111/ceo.12664. PMID: 26432996. |
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date |
2015-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
identifier |
https://doi.org/10.1111/ceo.12664 https://pubmed.ncbi.nlm.nih.gov/26432996 |
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http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21822 https://portal.issn.org/resource/ISSN/1442-9071 https://portal.issn.org/resource/ISSN/1442-6404 |
language |
English |
source |
https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/ |
title |
Targeted exome sequencing identified two novel truncation mutations in GPR98 causing Usher syndrome |
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