Evidence for linkage on chromosome 4p16.1 in Type 1 diabetes Danish families and complete mutation scanning of the WFS1 (Wolframin) gene. (Q47982108)

7 February 2018

title

Evidence for linkage on chromosome 4p16.1 in Type 1 diabetes Danish families and complete mutation scanning of the WFS1 (Wolframin) gene. (English)

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7 February 2018

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2

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Flemming Pociot

5

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author name string

Z M Larsen

1

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O P Kristiansen

3

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J Nerup

4

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Danish IDDM Epidemiology and Genetics Group

6

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Danish Study Group of IDDM in Childhood

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publication date

1 March 2004

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published in

Diabetic Medicine

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7 February 2018

volume

21

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7 February 2018

issue

3

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7 February 2018

page(s)

218-222

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7 February 2018

Genetics of type 1 diabetes mellitus

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A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome)

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Missense variations of the gene responsible for Wolfram syndrome (WFS1/wolframin) in Japanese: possible contribution of the Arg456His mutation to type 1 diabetes as a nonautoimmune genetic basis

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21 January 2018

Identifiers

DOI

1 reference

7 February 2018

PubMed ID

15008830

1 reference

7 February 2018