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- Title
Autosomal dominant transmission of diabetes and congenital hearing impairment secondary to a missense mutation in the WFS1 gene.
- Authors
Valéro, R; Bannwarth, S; Roman, S; Paquis-Flucklinger, V; Vialettes, B
- Abstract
Mutations of the WFS1 gene have been implicated in autosomal dominant diseases, such as low-frequency sensorineural hearing impairment (LFSNHI) and/or diabetes mellitus and/or optic atrophy. The aim was to investigate WFS1 gene sequences in a family with diabetes mellitus and hearing impairment.
- Publication
Diabetic medicine : a journal of the British Diabetic Association, 2008, Vol 25, Issue 6, p657
- ISSN
1464-5491
- Publication type
Journal Article
- DOI
10.1111/j.1464-5491.2008.02448.x