𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Phenotype of DFNA11: A Nonsyndromic Hearing Loss Caused by a Myosin VIIA Mutation

✍ Scribed by Yuya Tamagawa; Kazuhiro Ishikawa; Kotaro Ishikawa; Takashi Ishida; Ken Kitamura; Shinji Makino; Tadahiko Tsuru; Keiichi Ichimura


Book ID
110083929
Publisher
John Wiley and Sons
Year
2002
Tongue
English
Weight
146 KB
Volume
112
Category
Article
ISSN
0023-852X

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


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