Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a gene responsible in Japanese
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2001-07-01
著者
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SHINKAWA HIDEICHI
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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Usami Shinichi
Department Of Otolaryngology Shinshu University School Of Medicine
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USAMI Shin-ichi
Department of Otorhinolaryngology, Shinshu University School of Medicine
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Usami S
Shinshu Univ. School Of Medicine Matsumoto Jpn
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Usami Shin-ichi
Department Of Otorhinolaryngology Shinshu University School Of Medicine
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Abe Satoko
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science
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ABE Satoko
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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KIMBERLING William
Department of Genetics, Boys Town National Research Hospital
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AKITA Jiro
Department of Otorhinolaryngology, Hirosaki University School of Medicine
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Akita Jiro
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
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Shinkawa Hideichi
Department Of Otorhinolaryngology Hirosaki University School Of Medicine
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Shinkawa Hideichi
Department Of Otolaryngology Hirosaki University School Of Medicine
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Kimberling William
Department Of Genetics Boys Town National Research Hospital
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- Mutations in the gene encoding KIAA1199 protein, an inner-ear protein expressed in Deiters' cells and the fibrocytes, as the cause of nonsyndromic hearing loss
- Construction and characterization of a vestibular-specific cDNA library using T7-based RNA amplification
- Neurotransmission in the vestibular endorgans : Glutamatergic transmission in the afferent synapses of hair cells
- Genetic features of hearing loss associated with ear anomalies : PDS and EYA1 mutation analysis
- Clinical and genetic features of nonsyndromic autosomal dominant sensorineural hearing loss : KCNQ4 is a gene responsible in Japanese
- Rapid mass screening method and counseling for the 1555A'G mitochondrial mutation