reference/1825497

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1825497

Outgoing Links

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issn	1750-1172
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pageRange	57-
publicationName	Orphanet Journal of Rare Diseases
startingPage	57
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bibliographicCitation	Synofzik M, Schüle R, Schulze M, Gburek-Augustat J, Schweizer R, Schirmacher A, Krägeloh-Mann I, Gonzalez M, Young P, Züchner S, Schöls L, Bauer P. Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts. Orphanet Journal of Rare Diseases. 2014 Apr 17;9(1):57. doi: 10.1186/1750-1172-9-57.
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date	2014-04-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1186/1750-1172-9-57 https://pubmed.ncbi.nlm.nih.gov/24742043 https://pubmed.ncbi.nlm.nih.gov/PMC4021831
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://scigraph.springernature.com/ https://www.crossref.org/
title	Phenotype and frequency of STUB1 mutations: next-generation screenings in Caucasian ataxia and spastic paraplegia cohorts
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Incoming Links

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Total number of triples: 48.