A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
about
A meta-analysis and systematic review of the prevalence of mitochondrially encoded 12S RNA in the general population: Is there a role for screening neonates requiring aminoglycosides?Genetic Epidemiology of Mitochondrial Pathogenic Variants Causing Nonsyndromic Hearing Loss in a Large Cohort of South Indian Hearing Impaired Individuals.Complete mitochondrial genome analysis and clinical documentation of a five-generational Indian family with mitochondrial 1555A>G mutation and postlingual hearing loss.
P2860
A maternal hereditary deafness pedigree of the A1555G mitochondrial mutation, causing aminoglycoside ototoxicity predisposition.
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年学术文章
@wuu
2008年学术文章
@zh
2008年学术文章
@zh-cn
2008年学术文章
@zh-hans
2008年学术文章
@zh-my
2008年学术文章
@zh-sg
2008年學術文章
@yue
2008年學術文章
@zh-hant
name
A maternal hereditary deafness ...... de ototoxicity predisposition.
@en
A maternal hereditary deafness ...... de ototoxicity predisposition.
@nl
type
label
A maternal hereditary deafness ...... de ototoxicity predisposition.
@en
A maternal hereditary deafness ...... de ototoxicity predisposition.
@nl
prefLabel
A maternal hereditary deafness ...... de ototoxicity predisposition.
@en
A maternal hereditary deafness ...... de ototoxicity predisposition.
@nl
P2093
P2860
P1476
A maternal hereditary deafness ...... de ototoxicity predisposition.
@en
P2093
P2860
P304
P356
10.1017/S0022215107001648
P577
2008-02-19T00:00:00Z