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10371528
Source:
http://linkedlifedata.com/resource/pubmed/id/10371528
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pubmed-article:10371528
rdf:type
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pubmed-article:10371528
lifeskim:mentions
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lifeskim:mentions
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lifeskim:mentions
umls-concept:C2827424
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pubmed-article:10371528
pubmed:issue
9
lld:pubmed
pubmed-article:10371528
pubmed:dateCreated
1999-7-15
lld:pubmed
pubmed-article:10371528
pubmed:abstractText
To characterize the nature of CACNA1A mutations in episodic ataxia type 2 (EA2), to search for mutations in sporadic cases, and to delineate better the clinical spectrum.
lld:pubmed
pubmed-article:10371528
pubmed:language
eng
lld:pubmed
pubmed-article:10371528
pubmed:journal
http://linkedlifedata.com/r...
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pubmed-article:10371528
pubmed:citationSubset
AIM
lld:pubmed
pubmed-article:10371528
pubmed:status
MEDLINE
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pubmed-article:10371528
pubmed:month
Jun
lld:pubmed
pubmed-article:10371528
pubmed:issn
0028-3878
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pubmed-article:10371528
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pubmed-author:PerroutyBB
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pubmed-article:10371528
pubmed:issnType
Print
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pubmed-article:10371528
pubmed:day
10
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pubmed-article:10371528
pubmed:volume
52
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pubmed-article:10371528
pubmed:owner
NLM
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pubmed-article:10371528
pubmed:authorsComplete
Y
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pubmed-article:10371528
pubmed:pagination
1816-21
lld:pubmed
pubmed-article:10371528
pubmed:dateRevised
2006-11-15
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pubmed-article:10371528
pubmed:meshHeading
pubmed-meshheading:10371528...
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lld:pubmed
pubmed-article:10371528
pubmed:year
1999
lld:pubmed
pubmed-article:10371528
pubmed:articleTitle
High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
lld:pubmed
pubmed-article:10371528
pubmed:affiliation
INSERM U25, Faculté de Médecine Necker, Paris, France.
lld:pubmed
pubmed-article:10371528
pubmed:publicationType
Journal Article
lld:pubmed
pubmed-article:10371528
pubmed:publicationType
Research Support, Non-U.S. Gov't
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pubmed-article:10371528
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pubmed-article:10371528
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