reference/18051269

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/18051269

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endingPage	3469
issn	0964-6906 1460-2083
issueIdentifier	18
pageRange	3462-3469
publicationName	Human Molecular Genetics
startingPage	3462
bibliographicCitation	Attali R, Warwar N, Israel A, Gurt I, McNally E, Puckelwartz M, Glick B, Nevo Y, Ben-Neriah Z, Melki J. Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis. Hum Mol Genet. 2009 Sep 15;18(18):3462–9. doi: 10.1093/hmg/ddp290. PMID: 19542096.
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date	2009-06-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/19542096 https://doi.org/10.1093/hmg/ddp290
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis
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