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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Tatsuo Matsunaga

Laboratory of Auditory Disorders

National Institute of Sensory Organs

National Tokyo Medical Center

Tokyo

Japan

[email]@kankakuki.go.jp

Name/email consistency: high

 
 
 
 
 
 
 

Affiliation

  • Laboratory of Auditory Disorders, National Institute of Sensory Organs, National Tokyo Medical Center, Tokyo, Japan. 2006 - 2012

References

  1. In silico modeling of the pore region of a KCNQ4 missense mutant from a patient with hearing loss. Namba, K., Mutai, H., Kaneko, H., Hashimoto, S., Matsunaga, T. BMC. Res. Notes (2012) [Pubmed]
  2. Systematic analysis of mitochondrial genes associated with hearing loss in the Japanese population: dHPLC reveals a new candidate mutation. Mutai, H., Kouike, H., Teruya, E., Takahashi-Kodomari, I., Kakishima, H., Taiji, H., Usami, S., Okuyama, T., Matsunaga, T. BMC Med. Genet. (2011) [Pubmed]
  3. Value of genetic testing in the otological approach for sensorineural hearing loss. Matsunaga, T. Keio. J. Med (2009) [Pubmed]
  4. Phenotypic consequences in a Japanese family having branchio-oto-renal syndrome with a novel frameshift mutation in the gene EYA1. Matsunaga, T., Okada, M., Usami, S., Okuyama, T. Acta Otolaryngol. (2007) [Pubmed]
  5. Clinical course of hearing and language development in GJB2 and non-GJB2 deafness following habilitation with hearing aids. Matsunaga, T., Hirota, E., Bito, S., Niimi, S., Usami, S. Audiol. Neurootol. (2006) [Pubmed]
 
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