功能: disease:Defects in SURF1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions that is commonly associated with systemic cytochrome c oxidase (COX) deficiency.,function:Probably involved in the biogenesis of the COX complex.,similarity:Belongs to the SURF1 family.,
相关产品: YT4471,KA3748C,RS0001,RS0002,YM3028,YM3029
细胞定位: Mitochondrion inner membrane ; Multi-pass membrane protein .
功能: disease:Defects in SURF1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions that is commonly associated with systemic cytochrome c oxidase (COX) deficiency.,function:Probably involved in the biogenesis of the COX complex.,similarity:Belongs to the SURF1 family.,
相关产品: YT4471,KA3748C,RS0001,RS0002,YM3028,YM3029
细胞定位: Mitochondrion inner membrane ; Multi-pass membrane protein .