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WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis.
Kobayashi M, Miyagawa M, Nishio SY, Moteki H, Fujikawa T, Ohyama K, Sakaguchi H, Miyanohara I, Sugaya A, Naito Y, Morita SY, Kanda Y, Takahashi M, Ishikawa K, Nagano Y, Tono T, Oshikawa C, Kihara C, Takahashi H, Noguchi Y, Usami SI. Kobayashi M, et al. Among authors: usami si. PLoS One. 2018 Mar 12;13(3):e0193359. doi: 10.1371/journal.pone.0193359. eCollection 2018. PLoS One. 2018. PMID: 29529044 Free PMC article.
Prevalence of mitochondrial gene mutations among hearing impaired patients.
Usami S, Abe S, Akita J, Namba A, Shinkawa H, Ishii M, Iwasaki S, Hoshino T, Ito J, Doi K, Kubo T, Nakagawa T, Komiyama S, Tono T, Komune S. Usami S, et al. J Med Genet. 2000 Jan;37(1):38-40. doi: 10.1136/jmg.37.1.38. J Med Genet. 2000. PMID: 10633132 Free PMC article.
360 results