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Publication year
2003Source
Journal of Investigative Dermatology, 121, 5, (2003), pp. 1035-8ISSN
Publication type
Article / Letter to editor

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Organization
Dermatology
Journal title
Journal of Investigative Dermatology
Volume
vol. 121
Issue
iss. 5
Page start
p. 1035
Page end
p. 8
Subject
UMCN 4.2: Chronic inflammation and autoimmunity; UMCN 5.1: Genetic defects of metabolismAbstract
We studied three families suffering from nail abnormalities who had previously been diagnosed as pachyonychia congenita. No keratin gene mutations were detected. Sequencing of connexin 30 (GJB6 gene) in these patients identified heterozygous missense mutations G11R and A88V that are known to be associated with Clouston syndrome. This unexpected finding expands the Clouston syndrome phenotype and suggests that some patients diagnosed with pachyonychia may in fact be suffering from Clouston syndrome.
This item appears in the following Collection(s)
- Academic publications [227695]
- Electronic publications [108794]
- Faculty of Medical Sciences [87091]
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