𝔖 Bobbio Scriptorium
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Mutations in the WFS1 gene and low frequency hearing loss

✍ Scribed by Matthew Whitley; Megha Garg; Xue Liu; Xiaomei Ouyang


Book ID
116814945
Publisher
SAGE Publications
Year
2009
Tongue
English
Weight
73 KB
Volume
141
Category
Article
ISSN
0194-5998

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πŸ“œ SIMILAR VOLUMES


Additional heterozygous 2507A>C mutation
✍ Taro Fujikawa; Yoshihiro Noguchi; Taku Ito; Masatoki Takahashi; Ken Kitamura πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 230 KB

## Abstract ## Objectives/Hypothesis: To describe the audiological profiles in a Japanese family with autosomal dominant hereditary sensorineural hearing loss (SNHL) and to identify the causative gene. ## Study Design: A family study at an academic tertiary referral center. ## Methods: A famil