De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring.
about
De novo mtDNA point mutations are common and have a low recurrence risk.Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckThree families with 'de novo' m.3243A > G mutation.[Diabetes mellitus associated with the mitochondrial mutation A3243G: frequency and clinical presentation].
P2860
De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring.
description
2001 nî lūn-bûn
@nan
2001 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2001 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2001年の論文
@ja
2001年学术文章
@wuu
2001年学术文章
@zh-cn
2001年学术文章
@zh-hans
2001年学术文章
@zh-my
2001年学术文章
@zh-sg
2001年學術文章
@yue
name
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@ast
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@en
type
label
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@ast
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@en
prefLabel
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@ast
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@en
P2093
P2860
P1476
De novo mutation in the mitoch ...... ing in MELAS in the offspring.
@en
P2093
P2860
P356
10.1046/J.1440-1754.2001.00611.X
P577
2001-02-01T00:00:00Z