Mitochondrial encephalomyopathies.

Mitochondrial encephalomyopathies.

Item
http://www.wikidata.org/entity/Q35085834
The in-depth evaluation of suspected mitochondrial diseaseRisk factors of ocular involvement in children with mitochondrial respiratory chain complex defect.The myelin mutants as models to study myelin repair in the leukodystrophies.Extensive remyelination of the CNS leads to functional recovery.Potentially diagnostic electron paramagnetic resonance spectra elucidate the underlying mechanism of mitochondrial dysfunction in the deoxyguanosine kinase deficient rat model of a genetic mitochondrial DNA depletion syndromeA possible role for mitochondrial dysfunction in migraine.Inherited and acquired disorders of myelin: The underlying myelin pathology.Functional polypeptides can be synthesized from human mitochondrial transcripts lacking termination codonsA novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency.Maternally inherited deafness and unusual phenotypic manifestations associated with A3243G mitochondrial DNA mutation.Alteration in the copy number of mitochondrial DNA in leukocytes of patients with mitochondrial encephalomyopathies.
P2860

Mitochondrial encephalomyopathies.

Item
http://www.wikidata.org/entity/Q35085834
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Mitochondrial encephalomyopathies.
@ast
Mitochondrial encephalomyopathies.
@en
type
label
Mitochondrial encephalomyopathies.
@ast
Mitochondrial encephalomyopathies.
@en
prefLabel
Mitochondrial encephalomyopathies.
@ast
Mitochondrial encephalomyopathies.
@en
P1433
P1476
P2093
P2860
P304
P31
P356
P433
P478
P577
P698
P356
P1433
P1476
Mitochondrial encephalomyopathies.
@en
P2093
P2860
P304
P31
P356
P433
P478
P577
P698