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Sondheimer, NealPerson Why?
Analysis of cerebrospinal fluid mitochondrial DNA levels in Alzheimer disease.Academic Article Why?
Maternally inherited hypertrophic cardiomyopathy: a manifestation of mitochondrial DNA mutations--clinical course in two families.Academic Article Why?
MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.Academic Article Why?
Mitochondrial DNA depletion and dGK gene mutations.Academic Article Why?
Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination.Academic Article Why?
Mitochondrial DNA, nuclear context, and the risk for carcinogenesis.Academic Article Why?
Normal mitochondrial DNA and respiratory chain activity in familial dysautonomia fibroblasts.Academic Article Why?
Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.Academic Article Why?
Novel mutation in DGUOK in hepatocerebral mitochondrial DNA depletion syndrome associated with cystathioninuria.Academic Article Why?
Role of MHC class I in immune surveillance of mitochondrial DNA integrity.Academic Article Why?
Transfer of a mitochondrial DNA fragment to MCOLN1 causes an inherited case of mucolipidosis IV.Academic Article Why?
Origins and functional consequences of somatic mitochondrial DNA mutations in human cancer.Academic Article Why?
Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high.Academic Article Why?
Answers to missing mtDNA found at last.Academic Article Why?
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