reference/7281783

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/7281783

Outgoing Links

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contentType	Journal Article\|Research Support, N.I.H., Extramural\|Research Support, Non-U.S. Gov't
endingPage	5798
issn	0006-4971 1528-0020
issueIdentifier	22
pageRange	5794-5798
publicationName	Blood
startingPage	5794
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bibliographicCitation	Zhang K, Jordan MB, Marsh RA, Johnson JA, Kissell D, Meller J, Villanueva J, Risma KA, Wei Q, Klein PS, Filipovich AH. Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH. Blood. 2011 Nov 24;118(22):5794–8. PMID: 21881043; PMCID: PMC3228496.
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date	2011-11-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/21881043 https://doi.org/10.1182/blood-2011-07-370148 https://pubmed.ncbi.nlm.nih.gov/PMC3228496
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH
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