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Nonsyndromic Hearing Loss Caused by a Mitochondrial T7511C Mutation

✍ Scribed by Kotaro Ishikawa; Yuya Tamagawa; Katsumasa Takahashi; Hiroshi Kimura; Jun Kusakari; Akira Hara; Keiichi Ichimura


Book ID
110084118
Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
96 KB
Volume
112
Category
Article
ISSN
0023-852X

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DFNA8/12 caused by TECTA mutations is th
✍ Michael S. Hildebrand; MatΓ­as MorΓ­n; Nicole C. Meyer; Fernando Mayo; Silvia Moda πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 476 KB

The prevalence of DFNA8/DFNA12 (DFNA8/12), a type of autosomal dominant nonsyndromic hearing loss (ADNSHL), is unknown as comprehensive population-based genetic screening has not been conducted. We therefore completed unbiased screening for TECTA mutations in a Spanish cohort of 372 probands from AD