reference/257819

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/257819

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	604
issn	0003-9942
issueIdentifier	4
pageRange	598-604
publicationName	Archives of Neurology
startingPage	598
bibliographicCitation	Birouk N, Azzedine H, Dubourg O, Muriel MP, Benomar A, Hamadouche T, Maisonobe T, Ouazzani R, Brice A, Yahyaoui M, Chkili T, Le Guern E. Phenotypical features of a Moroccan family with autosomal recessive Charcot-Marie-Tooth disease associated with the S194X mutation in the GDAP1 gene. Arch Neurol. 2003 Apr;60(4):598–604. doi: 10.1001/archneur.60.4.598. PMID: 12707075.
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date	2003-04-01^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1001/archneur.60.4.598 https://pubmed.ncbi.nlm.nih.gov/12707075
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Phenotypical Features of a Moroccan Family With Autosomal Recessive Charcot-Marie-Tooth Disease Associated With the S194X Mutation in the GDAP1 Gene
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Incoming Links

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