reference/10446398

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10446398

Outgoing Links

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contentType	Journal Article\|Research Support, Non-U.S. Gov't
endingPage	574
issn	1460-2083 0964-6906
issueIdentifier	4
pageRange	567-574
publicationName	Human Molecular Genetics
startingPage	567
bibliographicCitation	Abbas N, Lücking CB, Ricard S, Dürr A, Bonifati V, De Michele G, Bouley S, Vaughan JR, Gasser T, Marconi R, Broussolle E, Brefel-Courbon C, Harhangi BS, Oostra BA, Fabrizio E, Böhme GA, Pradier L, Wood NW, Filla A, Meco G, Denefle P, Agid Y, Brice A. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease. Hum Mol Genet. 1999 Apr;8(4):567–74. doi: 10.1093/hmg/8.4.567. PMID: 10072423.
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date	1999-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1093/hmg/8.4.567 https://pubmed.ncbi.nlm.nih.gov/10072423
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease
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