## Abstract Mutations in the __WFS1__ gene have been reported in Wolfram syndrome (WS), an autosomal recessive disorder defined by early onset of diabetes mellitus (DM) and progressive optic atrophy. Because of the low prevalence of this syndrome and the recent identification of the __WFS1__ gene,
✦ LIBER ✦
Wolfram syndrome in the Polish population: novel mutations and genotype–phenotype correlation
✍ Scribed by A. Zmyslowska; M. Borowiec; K. Antosik; M. Szalecki; A. Stefanski; B. Iwaniszewska; M. Jedrzejczyk; I. Pietrzak; W. Mlynarski
- Book ID
- 108704965
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 167 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0300-0664
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