Pathogenic mtDNA mutations causing mitochondrial myopathy: the need for muscle biopsy
Pathogenic mitochondrial tRNA (mt-tRNA) gene mutations represent a prominent cause of primary mitochondrial DNA (mtDNA)-related disease despite accounting for only 5%-10% of the mitochondrial genome.(1,2) Although some common mt-tRNA mutations, such as the m.3243A>G mutation, exist, the major...
Główni autorzy: | Hardy, S, Blakely, E, Purvis, A, Rocha, M, Ahmed, S, Falkous, G, Poulton, J, Rose, M, O'Mahony, O, Bermingham, N, Dougan, C, Ng, Y, Horvath, R, Turnbull, D, Gorman, G, Taylor, R |
---|---|
Format: | Journal article |
Język: | English |
Wydane: |
American Academy of Neurology
2016
|
Podobne zapisy
-
Aerobic Exercise Training in Patients With mtDNA-Related Mitochondrial Myopathy
od: Tina Dysgaard Jeppesen
Wydane: (2020-05-01) -
Biallelic Variants in <i>ENDOG</i> Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions
od: Alessia Nasca, i wsp.
Wydane: (2022-03-01) -
CPEO and Mitochondrial Myopathy in a Patient with DGUOK Compound Heterozygous Pathogenetic Variant and mtDNA Multiple Deletions
od: V. Montano, i wsp.
Wydane: (2019-01-01) -
A proteomic approach to mtDNA depletion
od: Adams, S, i wsp.
Wydane: (2004) -
Information for genetic management of mtDNA disease: Sampling pathogenic mtDNA mutants in the human germline and in placenta
od: Marchington, D, i wsp.
Wydane: (2010)