reference/9456006

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9456006

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't\|Research Support, N.I.H., Extramural
endingPage	4576
issn	1460-2083 0964-6906
issueIdentifier	20
pageRange	ddw286-4576
publicationName	Human Molecular Genetics
startingPage	ddw286
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bibliographicCitation	Shin JW, Kim KH, Chao MJ, Atwal RS, Gillis T, MacDonald ME, Gusella JF, Lee JM. Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9. Hum Mol Genet. 2016 Oct 15;25(20):4566–76. PMID: 28172889; PMCID: PMC6078600.
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date	2016-09-15^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC6078600 https://doi.org/10.1093/hmg/ddw286 https://pubmed.ncbi.nlm.nih.gov/28172889
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9
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