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Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation

✍ Scribed by Katsuhiko Kobayashi; Tomohiro Oguchi; Kenji Asamura; Maiko Miyagawa; Satoshi Horai; Satoko Abe; Shin-ichi Usami

Book ID: 116223201
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 252 KB
Volume: 32
Category: Article
ISSN: 0385-8146
DOI: 10.1016/j.anl.2005.01.010

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