about
The in-depth evaluation of suspected mitochondrial diseaseClinical mitochondrial genetics.Neuroimaging of mitochondrial disease.D-2-Hydroxyglutaric aciduria: biochemical marker or clinical disease entity?Infantile leukoencephalopathy owing to mitochondrial enzyme dysfunction.A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency.
P2860
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
Magnetic resonance imaging in lactic acidosis.
@en
type
label
Magnetic resonance imaging in lactic acidosis.
@en
prefLabel
Magnetic resonance imaging in lactic acidosis.
@en
P2093
P2860
P356
P1476
Magnetic resonance imaging in lactic acidosis.
@en
P2093
van der Knaap MS
P2860
P2888
P304
P356
10.1007/BF01799114
P577
1996-01-01T00:00:00Z