Mitochondrial anomalies in a Swiss family with autosomal dominant myoglobinuria.
Am J Med Genet
; 69(4): 365-9, 1997 Apr 14.
Article
in En
| MEDLINE
| ID: mdl-9098484
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Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genes, Dominant
/
Myoglobinuria
Type of study:
Prognostic_studies
Limits:
Adolescent
/
Adult
/
Child
/
Female
/
Humans
/
Male
Country/Region as subject:
Europa
Language:
En
Journal:
Am J Med Genet
Year:
1997
Type:
Article
Affiliation country:
Switzerland