Source:http://linkedlifedata.com/resource/pubmed/id/10408526
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1999-8-9
|
| pubmed:commentsCorrections | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
AIM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:month |
Jul
|
| pubmed:issn |
0028-3878
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
13
|
| pubmed:volume |
53
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
3-4
|
| pubmed:dateRevised |
2005-11-17
|
| pubmed:meshHeading |
pubmed-meshheading:10408526-Amino Acid Substitution,
pubmed-meshheading:10408526-Calcium Channels,
pubmed-meshheading:10408526-Cerebellar Ataxia,
pubmed-meshheading:10408526-Hemiplegia,
pubmed-meshheading:10408526-Humans,
pubmed-meshheading:10408526-Migraine Disorders,
pubmed-meshheading:10408526-Point Mutation
|
| pubmed:year |
1999
|
| pubmed:articleTitle |
CACNA1A mutations: hemiplegic migraine, episodic ataxia type 2, and the others.
|
| pubmed:publicationType |
Editorial,
Comment,
Review
|