reference/23431134

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/23431134

Outgoing Links

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endingPage	284
issn	1468-6244
issueIdentifier	4
pageRange	281-284
publicationName	Journal of Medical Genetics
startingPage	281
bibliographicCitation	Depienne C, Fedirko E, Forlani S, Cazeneuve C, Ribai P, Feki I, Tallaksen C, Nguyen K, Stankoff B, Ruberg M, Stevanin G, Durr A, Brice A. Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia. Journal of Medical Genetics. 2007 Apr 01;44(4):281–4. doi: 10.1136/jmg.2006.046425.
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date	2007-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1136/jmg.2006.046425 https://pubmed.ncbi.nlm.nih.gov/PMC2598038 https://pubmed.ncbi.nlm.nih.gov/17098887
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Exon deletions of SPG4 are a frequent cause of hereditary spastic paraplegia
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Incoming Links

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Total number of triples: 64.