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A novel mutation of the doublecortin gene in Japanese patients with X-linked lissencephaly and subcortical band heterotopia.

Authors: Kato, M  Kimura, T  Lin, C  Ito, A  Kodama, S  Morikawa, T  Soga, T  Hayasaka, K 
Citation: Kato M, etal., Hum Genet. 1999 Apr;104(4):341-4.
Pubmed: (View Article at PubMed) PMID:10369164

The doublecortin (DCX) gene was recently found to be involved in patients with X-linked lissencephaly and subcortical band heterotopia or double cortex syndrome. We have studied the coding regions of the DCX gene in 11 Japanese patients with cortical dysplasia and have identified three different mutations (R186C in exon 3, R272X and R303X in exon 5) in four sporadic female cases. R272X, which has been detected in two unrelated cases, is a novel mutation. Although the number of cases studied remains limited, exon 5 may be a common mutational site in Japanese patients in contrast to many previous reports concerning exons 2 and 3.

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CRRD Object Information
CRRD ID: 12904717
Created: 2017-05-18
Species: All species
Last Modified: 2017-05-18
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.