Follow-up in carriers of the 'MELAS' mutation without strokes.
about
Central nervous system manifestations of mitochondrial disorders.De novo mutation in the mitochondrial tRNALeu(UUR) gene (A3243G) with rapid segregation resulting in MELAS in the offspring.Chronic kidney disease, severe arterial and arteriolar sclerosis and kidney neoplasia: on the spectrum of kidney involvement in MELAS syndromeClinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.Renal manifestations of genetic mitochondrial disease.Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
P2860
Follow-up in carriers of the 'MELAS' mutation without strokes.
description
1998 nî lūn-bûn
@nan
1998年の論文
@ja
1998年論文
@yue
1998年論文
@zh-hant
1998年論文
@zh-hk
1998年論文
@zh-mo
1998年論文
@zh-tw
1998年论文
@wuu
1998年论文
@zh
1998年论文
@zh-cn
name
Follow-up in carriers of the 'MELAS' mutation without strokes.
@en
type
label
Follow-up in carriers of the 'MELAS' mutation without strokes.
@en
prefLabel
Follow-up in carriers of the 'MELAS' mutation without strokes.
@en
P2093
P356
P1433
P1476
Follow-up in carriers of the 'MELAS' mutation without strokes.
@en
P2093
Bachmann G
Dorndorf W
Reichmann H
Schachenmayr W
P356
10.1159/000007892
P577
1998-01-01T00:00:00Z