reference/27775939

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/27775939

Outgoing Links

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issn	2324-9269
issueIdentifier	3
pageRange	e1123-
publicationName	Molecular genetics & genomic medicine
startingPage	e1123
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bibliographicCitation	Abu‐Ameerh M, Mohammad H, Dardas Z, Barham R, Ali D, Bijawi M, Tawalbeh M, Amr S, Hatmal MM, Al‐Bdour M, Awidi A, Azab B. Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing. Molec Gen & Gen Med. 2020 Jan 22;8(3). doi: 10.1002/mgg3.1123.
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date	2020-01-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1002/mgg3.1123 https://pubmed.ncbi.nlm.nih.gov/31968401 https://pubmed.ncbi.nlm.nih.gov/PMC7057102
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Extending the spectrum of CLRN1‐ and ABCA4‐associated inherited retinal dystrophies caused by novel and recurrent variants using exome sequencing
discusses	http://id.nlm.nih.gov/mesh/M0027776 http://id.nlm.nih.gov/mesh/M0402029 http://id.nlm.nih.gov/mesh/M0013341 http://id.nlm.nih.gov/mesh/M0158383
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Incoming Links

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Total number of triples: 44.