Evidence for a founder mutation causing DFNA5 hearing loss in East Asians
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概要
- 論文の詳細を見る
- 2010-01-01
著者
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Park Hong-Joon
Soree Ear Clinic
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Kim Un-kyung
Department Of Biology College Of Natural Sciences Kyungpook National University
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Park Hong-joon
Soree Ear Clinics
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Kwon Tae-jun
Department Of Biology College Of Natural Sciences Kyungpook National University
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CHO Hyun-Ju
Department of Biology, College of Natural Sciences, Kyungpook National University
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BAEK Jeong-In
Department of Biology, College of Natural Sciences, Kyungpook National University
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BEN-YOSEF Tamar
Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders/National Institutes of Health (NIDCD/NIH)
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GRIFFITH Andrew
Otolaryngology Branch, National Institute on Deafness and Other Communication Disorders/National Institutes of Health (NIDCD/NIH)
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Cho Hyun-ju
Department Of Biology College Of Natural Sciences Kyungpook National University
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Baek Jeong-in
Department Of Biology College Of Natural Sciences Kyungpook National University
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders/national Institutes Of Health (nidcd/nih)
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Ben-yosef Tamar
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders/national Institutes Of Health (nidcd/nih)
関連論文
- Evidence for a founder mutation causing DFNA5 hearing loss in East Asians
- Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage
- Genome-wide SNP-based linkage analysis for ADNSHL families identifies novel susceptibility loci with positive evidence for linkage
- Amino acid 572 in TMC1 : hot spot or critical functional residue for dominant mutations causing hearing impairment
- Evidence for a founder mutation causing DFNA5 hearing loss in East Asians
- SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis