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The H syndrome is caused by mutations in the nucleoside transporter hENT3

Authors :
Molho-Pessach, Vered
Lerer, Israela
Abeliovich, Dvorah
Agha, Ziad
Libdeh, Abu
Broshtilova, Valentina
Elpeleg, Orly
Zlotgorski, Abraham
Source :
American Journal of Human Genetics. Oct 10, 2008, Vol. 83 Issue 4, p529, 6 p.
Publication Year :
2008

Abstract

The article discusses the causes, symptoms and effects of the H syndrome, the autosomal-recessive disorder that is caused by the mutations taking place in the nucleoside transporter hENT3. The disorder is shown to be characterized by cutaneous hyperpigmentation, hypertrichosis, hearing loss and fixed flexion contractures of the toe joints.

Details

Language :
English
ISSN :
00029297
Volume :
83
Issue :
4
Database :
Gale General OneFile
Journal :
American Journal of Human Genetics
Publication Type :
Academic Journal
Accession number :
edsgcl.188990380