Wolfram syndrome (WS) is a recessively inherited mendelian form of diabetes and neurodegeneration also known by the acronym DIDMOAD from the major clinical features, including diabetes insipidus, diabetes mellitus, optic atrophy, and deafness. Affected individuals may also show renal tract abnormali
β¦ LIBER β¦
Clinical and Molecular Genetic Analysis of 19 Wolfram Syndrome Kindreds Demonstrating a Wide Spectrum of Mutations in WFS1
β Scribed by Carol Hardy; Farhat Khanim; Rosarelis Torres; Martin Scott-Brown; Anneke Seller; Joanna Poulton; David Collier; Jeremy Kirk; Mihael Polymeropoulos; Farida Latif; Timothy Barrett
- Book ID
- 117853028
- Publisher
- American Society of Human Genetics
- Year
- 1999
- Tongue
- English
- Weight
- 809 KB
- Volume
- 65
- Category
- Article
- ISSN
- 0002-9297
- DOI
- 10.1086/302609
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