reference/21484933

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/21484933

Outgoing Links

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endingPage	1971
issn	1460-2156 0006-8950
issueIdentifier	Pt 7
pageRange	1959-1971
publicationName	Brain : a journal of neurology
startingPage	1959
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bibliographicCitation	Nicholson G, Lenk GM, Reddel SW, Grant AE, Towne CF, Ferguson CJ, Simpson E, Scheuerle A, Yasick M, Hoffman S, Blouin R, Brandt C, Coppola G, Biesecker LG, Batish SD, Meisler MH. Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P₂ phosphatase FIG4. Brain. 2011 Jul;134(Pt 7):1959–71. PMID: 21705420; PMCID: PMC3122378.
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date	2011-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/PMC3122378 https://doi.org/10.1093/brain/awr148 https://pubmed.ncbi.nlm.nih.gov/21705420
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Distinctive genetic and clinical features of CMT4J: a severe neuropathy caused by mutations in the PI(3,5)P2 phosphatase FIG4
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