(Q50435861)

14 March 2018

title

Congenital cataracts in two siblings with Wolfram syndrome. (English)

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14 March 2018

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Rebecca B Mets

1

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14 March 2018

Sarah B Emery

series ordinal

2

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14 March 2018

Marci M Lesperance

series ordinal

3

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14 March 2018

Marilyn B Mets

series ordinal

4

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14 March 2018

publication date

1 December 2010

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14 March 2018

published in

Ophthalmic Genetics

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14 March 2018

volume

31

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14 March 2018

issue

4

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14 March 2018

page(s)

227-229

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14 March 2018

A homozygous mutation in a novel zinc-finger protein, ERIS, is responsible for Wolfram syndrome 2

cites work

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2010.516056

Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2010.516056

Mutation analysis of the WFS1 gene in seven Danish Wolfram syndrome families; four new mutations identified

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2010.516056

Non-syndromic progressive hearing loss DFNA38 is caused by heterozygous missense mutation in the Wolfram syndrome gene WFS1

21 January 2018

1 reference

https://api.crossref.org/works/10.3109%2F13816810.2010.516056

10.3109/13816810.2010.516056

21 January 2018

Identifiers

DOI

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14 March 2018

PubMed ID

21067485

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14 March 2018