reference/10790734

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/10790734

Outgoing Links

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issn	1750-1326
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publicationName	Molecular Neurodegeneration
startingPage	3
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bibliographicCitation	Madero-Pérez J, Fdez E, Fernández B, Lara Ordóñez AJ, Blanca Ramírez M, Gómez-Suaga P, Waschbüsch D, Lobbestael E, Baekelandt V, Nairn AC, Ruiz-Martínez J, Aiastui A, López de Munain A, Lis P, Comptdaer T, Taymans J, Chartier-Harlin M, Beilina A, Gonnelli A, Cookson MR, Greggio E, Hilfiker S. Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation. Molecular Neurodegeneration. 2018 Jan 23;13(1):3. doi: 10.1186/s13024-018-0235-y.
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date	2018-01-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/s13024-018-0235-y https://pubmed.ncbi.nlm.nih.gov/PMC5778812 https://pubmed.ncbi.nlm.nih.gov/29357897
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/32784 https://portal.issn.org/resource/ISSN/1750-1326
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Parkinson disease-associated mutations in LRRK2 cause centrosomal defects via Rab8a phosphorylation
discusses	http://id.nlm.nih.gov/mesh/M000613241 http://id.nlm.nih.gov/mesh/M0479539 http://id.nlm.nih.gov/mesh/M0328226 http://id.nlm.nih.gov/mesh/M0492483
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Incoming Links

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Total number of triples: 64.