Amino acid 572 in TMC1 : hot spot or critical functional residue for dominant mutations causing hearing impairment
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概要
- 論文の詳細を見る
- 2009-03-01
著者
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Van Camp
Department Of Haematology And Immunology Free′ University Brussels′ Hokkaido University. Vol. 2.
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Griffith Andrew
Otolaryngology Branch National Institute On Deafness And Other Communication Disorders National Institutes Of Health
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Griffith Andrew
Otolaryngology Branch Nidcd/nih
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HILGERT Nele
Department of Medical Genetics, University of Antwerp (UA)
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MONAHAN Kelly
Otolaryngology Branch, NIDCD/NIH
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KURIMA Kiyoto
Otolaryngology Branch, NIDCD/NIH
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LI Cindy
Section on Hereditary Disorders of the Ear, House Ear Institute
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FRIEDMAN Rick
Section on Hereditary Disorders of the Ear, House Ear Institute
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Li Cindy
Section On Hereditary Disorders Of The Ear House Ear Institute
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Hilgert Nele
Department Of Medical Genetics University Of Antwerp (ua)
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Monahan Kelly
Otolaryngology Branch Nidcd/nih
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Kurima Kiyoto
Otolaryngology Branch Nidcd/nih
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Friedman Rick
Section On Hereditary Disorders Of The Ear House Ear Institute
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Van Camp
Department Of Medical Genetics University Of Antwerp (ua)
関連論文
- Selective initial in vivo homing pattern of 5T2 multiple myeloma′ cells in the C57BL/KalwRij mouse.
- 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
- Genome-wide analysis reveals a novel autosomal-recessive hearing loss locus DFNB80 on chromosome 2p16.1-p21