Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
about
Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotypeMitochondrial DNA sequence characteristics modulate the size of the genetic bottleneckClinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.Clinical Heterogeneity, Tissue Distribution, and Intergenerational Segregation of mtDNA Mutation A3243G.
P2860
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
description
2002 nî lūn-bûn
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name
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@en
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@nl
type
label
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@en
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@nl
prefLabel
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@en
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@nl
P2093
P2860
P1476
Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
@en
P2093
P2860
P304
P356
10.1034/J.1600-0404.2002.01172.X
P407
P577
2002-08-01T00:00:00Z