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Homozygous Exon 4 deletion in Parkin gene in a Korean family with autosomal recessive early onset parkinsonism
被引:6
作者:
Kim, JS
Lee, KS
Kim, YI
Lee, KH
Kim, HT
机构:
[1] Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
[2] Catholic Univ Korea, Dept Pharmacol, Coll Med, Seoul, South Korea
[3] Catholic Univ Korea, Neurosci Genome Res Ctr, Coll Med, Seoul, South Korea
关键词:
autosomal recessive juvenile parkinsonism;
parkin;
familial;
mutation;
exon;
D O I:
10.3349/ymj.2003.44.2.336
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The gene responsible for autosomal recessive parkinsonism, parkin, has recently been identified on chromosome 6q. It has been shown to be mutated in Japanese and European families, most of whom had early-onset parkinsonism. Here, we present a family with young-onset parkinsonism of an autosomal recessive inheritance. A homozygous exon 4 deletion in the parkin gene was found in 3 family members. To the best of the authors' knowledge, this is the first report in Korea of familial parkinsonism with the parkin gene mutation.
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页码:336 / 339
页数:4
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