The myoclonic epilepsy and ragged-red fiber mutation provides new insights into human mitochondrial function and genetics
Am J Hum Genet
.
1998 Apr;62(4):745-51.
doi: 10.1086/301813.
Author
A Chomyn
1
Affiliation
1
Division of Biology, California Institute of Technology, Pasadena, CA, USA. chomyn@seqaxp.bio.caltech.ed
PMID:
9529371
PMCID:
PMC1377051
DOI:
10.1086/301813
No abstract available
Publication types
Research Support, U.S. Gov't, P.H.S.
Review
MeSH terms
DNA, Mitochondrial*
Genome, Human
Humans
MERRF Syndrome / genetics*
MERRF Syndrome / pathology
Mitochondria / genetics*
Mitochondria / pathology
Mutation*
Substances
DNA, Mitochondrial
Grants and funding
GM11726/GM/NIGMS NIH HHS/United States