Prevalence of mitochondrial gene mutations among hearing impaired patients

The frequency of three mitochondrial point mutations, 1555A→G, 3243A→G, and 7445A→G, known to be associated with hearing impairment, was examined using restriction fragment length polymorphism (RFLP) analysis in two Japanese groups: (1) 319 unrelated SNHL outpatients (including 21 with aminoglycosid...

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Autori principali: 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.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Group 2000
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Original Articles
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1734443/
https://ncbi.nlm.nih.gov/pubmed/10633132
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.37.1.38
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