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A novel deficiency of mitochondrial ATPase of nuclear origin
J. Houštěk, P. Klement, D. Floryk
Human molecular genetics.
1999 ;
Roč. 8 (č. 11) :
s. 1967-1974.
Language English Country Great Britain
Document type Case Reports
Persistent link
https://www.medvik.cz/link/bmc00015487
Online
NLK
Free Medical Journals
from 1996 to 1 year ago
Open Access Digital Library
from 1996-01-01
- MeSH
- Cell Nucleus genetics MeSH
- Fibroblasts enzymology pathology MeSH
- Infant MeSH
- Humans MeSH
- Mitochondria enzymology pathology MeSH
- Abnormalities, Multiple enzymology etiology MeSH
- Infant, Newborn MeSH
- Metabolism, Inborn Errors enzymology genetics complications MeSH
- Check Tag
- Infant MeSH
- Humans MeSH
- Infant, Newborn MeSH
- Publication type
- Case Reports MeSH
Department of Bioenergetics Institute of Physiology Academy of Sciences of the Czech Republic Prague
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