reference/12432468

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/12432468

Outgoing Links

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contentType	Case Reports\|Journal Article\|Research Support, Non-U.S. Gov't
endingPage	100
issn	0009-9163 1399-0004
issueIdentifier	2
pageRange	99-100
publicationName	Clinical Genetics
startingPage	99
bibliographicCitation	Pratt VM, Dlouhy SR, Hodes ME. Pelizaeus-Merzbacher disease: a point mutation in exon 6 of the proteolipid protein (PLP) gene. Clin Genet. 1995 Feb;47(2):99–100. doi: 10.1111/j.1399-0004.1995.tb03932.x. PMID: 7541731.
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date	199502
identifier	https://pubmed.ncbi.nlm.nih.gov/7541731 https://doi.org/10.1111/j.1399-0004.1995.tb03932.x
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/3010 https://portal.issn.org/resource/ISSN/1399-0004 https://portal.issn.org/resource/ISSN/0009-9163
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Pelizaeus‐Merzbacher disease: a point mutation in exon 6 of the proteolipid protein (PLP) gene
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Incoming Links

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Total number of triples: 41.