Entry |
|
Name |
Mutation-caused aberrant Htt to electron transfer in Complex II
|
Definition |
HTT* -| CxII -> QH2 |
Expanded |
3064v1 -| (6389+6390+6391+6392) -> C00390 |
Class |
|
Type |
Variant
|
Pathway |
|
Disease |
|
Gene |
6389 | SDHA; succinate dehydrogenase complex flavoprotein subunit A |
6390 | SDHB; succinate dehydrogenase complex iron sulfur subunit B |
6391 | SDHC; succinate dehydrogenase complex subunit C |
6392 | SDHD; succinate dehydrogenase complex subunit D |
|
Variant |
|
Metabolite |
|
Reference |
|
Authors |
Bossy-Wetzel E, Petrilli A, Knott AB |
Title |
Mutant huntingtin and mitochondrial dysfunction. |
Journal |
|
Reference |
|
Authors |
Gu M, Gash MT, Mann VM, Javoy-Agid F, Cooper JM, Schapira AH |
Title |
Mitochondrial defect in Huntington's disease caudate nucleus. |
Journal |
|
Reference |
|
Authors |
Labbadia J, Morimoto RI |
Title |
Huntington's disease: underlying molecular mechanisms and emerging concepts. |
Journal |
|
Reference |
|
Authors |
Mochel F, Haller RG |
Title |
Energy deficit in Huntington disease: why it matters. |
Journal |
|
LinkDB |
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