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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2006-7-31
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pubmed:abstractText |
Dystonia is a heterogenous group of movement disorders whose clinical spectrum is very wide. At least 13 different genes and gene loci have been reported. While a 3-bp deletion in the DYT1 gene is the most frequent cause of early limb-onset, generalized dystonia, it has also been found in non-generalized forms of sporadic dystonia. An 18-bp deletion in the DYT1 gene has also been reported.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0022-510X
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pubmed:author |
|
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pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
247
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
35-7
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pubmed:dateRevised |
2007-5-10
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pubmed:meshHeading |
pubmed-meshheading:16631205-Adult,
pubmed-meshheading:16631205-Asian Continental Ancestry Group,
pubmed-meshheading:16631205-Dystonic Disorders,
pubmed-meshheading:16631205-European Continental Ancestry Group,
pubmed-meshheading:16631205-Humans,
pubmed-meshheading:16631205-India,
pubmed-meshheading:16631205-Malaysia,
pubmed-meshheading:16631205-Middle Aged,
pubmed-meshheading:16631205-Molecular Chaperones,
pubmed-meshheading:16631205-Mutation,
pubmed-meshheading:16631205-Sequence Deletion,
pubmed-meshheading:16631205-Singapore
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pubmed:year |
2006
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pubmed:articleTitle |
DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West.
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pubmed:affiliation |
Department of Neurology, National Neuroscience Institute, 11 Jalan Tan Tock Seng, Singapore 308433, Singapore.
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pubmed:publicationType |
Journal Article,
Comparative Study,
Research Support, Non-U.S. Gov't
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