Literature DB >> 11359069

A novel nonsense mutation of the GTP cyclohydrolase I gene in a family with dopa-responsive dystonia.

K M Hong1, Y S Kim, M K Paik.   

Abstract

We report a new nonsense mutation in the GTP cyclohydrolase I (GCH1) gene in a family with dopa-responsive dystonia. Two sisters and three children of the sisters are affected. The exons of the GCH1 gene were amplified by PCR and sequenced. The substitution of thymine for cytosine at nucleotide position 142 causing a nonsense mutation (Q48X) in exon 1 was identified in all of the five affected patients. There were three asymptomatic carriers of the mutation in the family. Copyright 2001 S. Karger AG, Basel

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Year:  2001        PMID: 11359069     DOI: 10.1159/000053355

Source DB:  PubMed          Journal:  Hum Hered        ISSN: 0001-5652            Impact factor:   0.444


  2 in total

1.  Dopa-responsive dystonia with a novel initiation codon mutation in the GCH1 gene misdiagnosed as cerebral palsy.

Authors:  Jae-Hyeok Lee; Chang-Seok Ki; Dae-Seong Kim; Jae-Wook Cho; Kyung-Phil Park; Seonhye Kim
Journal:  J Korean Med Sci       Date:  2011-09-01       Impact factor: 2.153

2.  Predisposition of genetic disease by modestly decreased expression of GCH1 mutant allele.

Authors:  Yo Sik Kim; Yong Bock Choi; Jeong Hwa Lee; Sei Hoon Yang; Ji Hyun Cho; Chang Ho Shin; Sang Do Lee; Moon Kee Paik; Kyeong Man Hong
Journal:  Exp Mol Med       Date:  2008-06-30       Impact factor: 8.718

  2 in total

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