Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation.
about
De novo mtDNA point mutations are common and have a low recurrence risk.Defective complex I assembly due to C20orf7 mutations as a new cause of Leigh syndrome.Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993Skewed segregation of the mtDNA nt 8993 (T-->G) mutation in human oocytes
P2860
Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation.
description
1996 nî lūn-bûn
@nan
1996年の論文
@ja
1996年論文
@yue
1996年論文
@zh-hant
1996年論文
@zh-hk
1996年論文
@zh-mo
1996年論文
@zh-tw
1996年论文
@wuu
1996年论文
@zh
1996年论文
@zh-cn
name
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@en
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@nl
type
label
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@en
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@nl
prefLabel
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@en
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@nl
P2093
P2860
P1476
Isolated case of mental retard ...... mitochondrial T8993G mutation.
@en
P2093
P2860
P304
P407
P577
1996-03-01T00:00:00Z