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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao The Laryngoscopearrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
The Laryngoscope
Article . 2011 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
The Laryngoscope
Article . 2011
HKU Scholars Hub
Article . 2012
Data sources: HKU Scholars Hub
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Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients?

Authors: Zha, Y.; Chen, X.-M.; Lam, C.-W.; Lee, S.-C.; Tong, S.-F.; Gao, Z.-Q.;

Is the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene due to a founder effect in Chinese head and neck paraganglioma patients?

Abstract

AbstractObjectives/Hypothesis:Three Chinese patients with head and neck paragangliomas have been reported to carry the c.3G>C mutation in the succinate dehydrogenase subunit D (SDHD) gene. In addition, in our hospital, two further patients were identified who have the same mutation. It is unclear whether the c.3G>C mutation in Chinese patients is a recurrent mutation or if it is due to a founder effect. We conducted haplotype analysis on these patients to answer this question.Study Design:Individual case‐control study.Methods:Germ‐line mutations were confirmed in the patients and their families examined in this study using direct sequencing. We also constructed and analyzed haplotypes in four Chinese families. Genotype frequencies were compared to the control group.Results:Three of four families shared the same haplotype, which rarely occurred in the control group. The last family shared a very short area on the physical map with the other three families.Conclusions:There is a founder effect in Chinese head and neck paraganglioma patients carrying the SDHD c.3G>C mutation.

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Keywords

Adult, Male, haplotype, China, Population, 610, Paraganglioma, paraganglioma, 616, Genetics, Humans, Point Mutation, Paraganglioma - Genetics, Germ-Line Mutation, Succinate Dehydrogenase - Genetics, Founder effect, Middle Aged, succinate dehydrogenase, Founder Effect, Head And Neck Neoplasms - Genetics, Succinate Dehydrogenase, Genetics, Population, Haplotypes, Head and Neck Neoplasms, Female, germ-line mutation, Microsatellite Repeats

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
3
Average
Average
Average