New mutations in TK2 gene associated with mitochondrial DNA depletion.
Pediatr Neurol
; 34(3): 177-85, 2006 Mar.
Article
in En
| MEDLINE
| ID: mdl-16504786
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Thymidine Kinase
/
DNA, Mitochondrial
/
DNA Mutational Analysis
/
Chromosome Aberrations
/
Mitochondrial Encephalomyopathies
/
Genes, Recessive
Type of study:
Diagnostic_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Language:
En
Journal:
Pediatr Neurol
Journal subject:
NEUROLOGIA
/
PEDIATRIA
Year:
2006
Document type:
Article
Affiliation country:
Italia
Country of publication:
Estados Unidos