Clinical and molecular survey in 124 Chinese patients with Leigh or Leigh-like syndrome.

Journal of inherited metabolic disease

Volumn 30, Issue 2, 2007, Pages 265-

  Zhang, Y ^a   Yang, Y L ^a   Sun, F ^a   Cai, X ^a   Qian, N ^a   Yuan, Y ^a   Wang, Z X ^a   Qi, Y ^a   Xiao, J X ^a   Wang, X Y ^a   Zhang, Y H ^a   Jiang, Y W ^a   Qin, J ^a   Wu, X R ^a  

^a PEKING UNIVERSITY FIRST HOSPITAL   (China)

Author keywords

[No Author keywords available]

Indexed keywords

MEMBRANE PROTEIN; MITOCHONDRIAL DNA; MITOCHONDRIAL PROTEIN; PYRUVATE DEHYDROGENASE; PYRUVATE DEHYDROGENASE E1ALPHA SUBUNIT; SURF 1 PROTEIN; SURF-1 PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ARTICLE; ASIAN; BRAIN; CHILD; COMPUTER ASSISTED TOMOGRAPHY; CYTOCHROME C OXIDASE DEFICIENCY; FEMALE; GENETIC VARIABILITY; GENETICS; HUMAN; INFANT; LEIGH DISEASE; MALE; MOTOR DYSFUNCTION; MUTATION; NEWBORN; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PATHOLOGY; POINT MUTATION; PRESCHOOL CHILD; RADIOGRAPHY;

ADOLESCENT; AGE OF ONSET; ASIAN CONTINENTAL ANCESTRY GROUP; BRAIN; CHILD; CHILD, PRESCHOOL; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; LEIGH DISEASE; MAGNETIC RESONANCE IMAGING; MALE; MEMBRANE PROTEINS; MITOCHONDRIAL PROTEINS; MOVEMENT DISORDERS; MUTATION; POINT MUTATION; PYRUVATE DEHYDROGENASE (LIPOAMIDE); TOMOGRAPHY, X-RAY COMPUTED; VARIATION (GENETICS);

EID: 34247558085     PISSN: None     EISSN: 15732665     Source Type: Journal    
DOI: 10.1007/s10545-006-0481-y     Document Type: Article

References (0)