SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway-Reference-Cited by-同舟云学术

SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway

Published:2009-03-31 Issue:12 Volume:18 Page:2257-2265
ISSN:1460-2083
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

Cliffe Simon T.,Kramer Jamie M.,Hussain Khalid,Robben Joris H.,de Jong Eiko K.,de Brouwer Arjan P.,Nibbeling Esther,Kamsteeg Erik-Jan,Wong Melanie,Prendiville Julie,James Chela,Padidela Raja,Becknell Charlie,van Bokhoven Hans,Deen Peter M.T.,Hennekam Raoul C.M.,Lindeman Robert,Schenck Annette,Roscioli Tony,Buckley Michael F.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/18/12/2257/17247225/ddp161.pdf

Reference41 articles.

1. The emerging genetic architecture of type 2 diabetes;Doria;Cell Metab.,2008

2. Beyond the beta cell in diabetes;Hattersley;Nat. Genet.,2006

3. Pigmented hypertrichotic dermatosis and insulin dependent diabetes, manifestations of a unique genetic disorder?;Prendiville;Pediatr. Dermatol.,2007

4. Diabetes mellitus, exocrine pancreatic deficiency, hypertrichosis, hyperpigmentation, and chronic inflammation. Confirmation of a syndrome;Hussain;Pediatr. Diabetes,2008

5. POEMS in childhood;Marina;Pediatr. Dermatol.,2006

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