Results 11 -
20
of
24
for
Leigh "syndrome," mitochondrial
Did you mean light "syndrome," mitochondrial?
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition COXPD12 gluRS glutamate tRNA ligase 2, mitochondrial glutamate--tRNA ligase KIAA1970 MSE1 Tests of EARS2 ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition EFG EFG1 EFGM EGF1 G translation elongation factor, mitochondrial GFM hEFG1 mitochondrial elongation factor G mitochondrial elongation ...
- ... lipoamide) beta pyruvate dehydrogenase E1 component subunit beta, mitochondrial pyruvate dehydrogenase, E1 beta polypeptide Tests of PDHB PubMed LEIGH SYNDROME, NUCLEAR; NULS PYRUVATE DEHYDROGENASE E1, SUBUNIT BETA; PDHB ...
- ... gene are related to the specific features of Leigh syndrome. More About This Health Condition ... succinate dehydrogenase complex flavoprotein subunit succinate dehydrogenase complex ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition BC1 (ubiquinol-cytochrome c reductase) synthesis-like BCS1 BCS1-like protein BCS1_HUMAN h-BCS1 Hs.6719 mitochondrial chaperone BCS1 mitochondrial complex III assembly Tests of ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition ... D, Cohen-Katsenelson K, Iancu TC, Manov I, Saada A, Sprecher E, Mandel H. Infantile mitochondrial hepatopathy is a cardinal feature of MEGDEL syndrome ( ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About This Health Condition ... Almannai M, Dai H, El-Hattab AW, Wong LJC. FBXL4-Related Encephalomyopathic Mitochondrial DNA Depletion Syndrome. 2017 Apr 6. In: Adam ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome More About ... PubMed PYRUVATE DEHYDROGENASE E1-ALPHA ...
- ... Kirby DM, Chow CW, Christodoulou J, Thorburn DR. Leigh syndrome: clinical ... Y. The T-C(8356) mitochondrial DNA mutation in a Japanese family. J Neurol. ...
- ... This Health Condition MedlinePlus Genetics provides information about Leigh syndrome ... PubMed PYRUVATE DEHYDROGENASE COMPLEX, COMPONENT ...