Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in theSDHDgene-Reference-Cited by-同舟云学术

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in theSDHDgene

Published:2001-05-04 Issue:3 Volume:31 Page:274-281
ISSN:1045-2257
Container-title:Genes, Chromosomes and Cancer
language:en
Short-container-title:Genes Chromosom. Cancer

Author:

Taschner Peter E.M.,Jansen Jeroen C.,Baysal Bora E.,Bosch Anne,Rosenberg Efraim H.,Bröcker-Vriends Annette H.J.T.,van der Mey Andel G.L.,van Ommen Gert-Jan B.,Cornelisse Cees J.,Devilee Peter

Funder

Dutch Cancer Society

Publisher

Wiley

Subject

Cancer Research,Genetics

Reference24 articles.

1. Repositioning the hereditary paraganglioma critical region on chromosome band 11q23;Baysal;Hum Genet,1999

2. Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma;Baysal;Science,2000

3. Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency;Bourgeron;Nat Genet,1995

4. Rearranged mitochondrial genomes are present in human oocytes;Chen;Am J Hum Genet,1995

5. Allelotype of head and neck paragangliomas: allelic imbalance is confined to the long arm of chromosome 11, the site of the predisposing locus PGL;Devilee;Genes Chromosomes Cancer,1994

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