Mitochondrial gene mutations and human diseases: a prolegomenon.
about
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees.Simultaneous occurrence of the 11778 (ND4) and the 9438 (COX III) mtDNA mutations in Leber hereditary optic neuropathy: molecular, biochemical, and clinical findings.
P2860
Mitochondrial gene mutations and human diseases: a prolegomenon.
description
1994 nî lūn-bûn
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1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Mitochondrial gene mutations and human diseases: a prolegomenon.
@en
Mitochondrial gene mutations and human diseases: a prolegomenon.
@nl
type
label
Mitochondrial gene mutations and human diseases: a prolegomenon.
@en
Mitochondrial gene mutations and human diseases: a prolegomenon.
@nl
prefLabel
Mitochondrial gene mutations and human diseases: a prolegomenon.
@en
Mitochondrial gene mutations and human diseases: a prolegomenon.
@nl
P2860
P1476
Mitochondrial gene mutations and human diseases: a prolegomenon.
@en
P2093
P2860
P304
P407
P577
1994-08-01T00:00:00Z