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A novel KCNQ4 one-base deletion in a large pedigree with hearing loss: implication for the genotype–phenotype correlation

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Year: 2006
Type: article
Study design: Observational Study
Source: Journal of Human Genetics
DOI: 10.1007/s10038-006-0384-7
Authors: Fumiaki Kamada, Shigeo Kure, Takayuki Kudo, Yoichi Suzuki, Takeshi Oshima, Akiko Ichinohe, Kanako Kojima, Tetsuya Niihori, Junko Kanno, Yoko Narumi, Ayumi Narisawa, Kumi Kato, Yoko Aoki, Katsuhisa Ikeda, Toshimitsu Kobayashi, Yoichi Matsubara
Institution: Tohoku University
Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics
Subfield: Sensory Systems
Field: Neuroscience
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: closed

Funders: Ministry of Education, Culture, Sports, Science and Technology, Japan Society for the Promotion of Science
OpenAlex ID: W2133845331
FWCI: 1.23
Cites: 21
Cited by: 55
Related to: 10
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