Literature DB >> 12728478

Homozygous exon 4 deletion in parkin gene in a Korean family with autosomal recessive early onset parkinsonism.

Joong-Seok Kim1, Kwang-Soo Lee, Yeong-In Kim, Kwon-Haeng Lee, Hong-Tae Kim.   

Abstract

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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Year:  2003        PMID: 12728478     DOI: 10.3349/ymj.2003.44.2.336

Source DB:  PubMed          Journal:  Yonsei Med J        ISSN: 0513-5796            Impact factor:   2.759


  1 in total

1.  Cardiac (123)I-metaiodobenzylguanidine Scintigraphy in a Patient with Familial Parkinsonism with Parkin Gene Mutation.

Authors:  Young-Do Kim; In-Uk Song; Joong-Seok Kim; Sung-Woo Chung; Kwang-Soo Lee
Journal:  J Mov Disord       Date:  2010-10-30
  1 in total

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