Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia

Neurogenetics

Volumn 10, Issue 4, 2009, Pages 337-345

  Wang, Kang ^a,b,c   Takahashi, Yuji ^c   Gao, Zong Liang ^d   Wang, Guo Xiang ^a   Chen, Xian Wen ^d   Goto, Jun ^c   Lou, Jin Ning ^a   Tsuji, Shoji ^c  

^a GRADUATE SCHOOL OF PEKING UNION MEDICAL COLLEGE   (China)

^b CHINA JAPAN FRIENDSHIP HOSPITAL   (China)

^c UNIVERSITY OF TOKYO   (Japan)

^d ANHUI MEDICAL UNIVERSITY   (China)

Author keywords

Gene chip; Leber hereditary optic neuropathy and dystonia (LDYT); Mitochondrion; ND3; Oxidative phosphorylation disorders

Indexed keywords

MT ND3 PROTEIN, HUMAN; MT-ND3 PROTEIN, HUMAN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE);

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; ANIMAL; ARTICLE; ASIAN; BRAIN; CHILD; DYSTONIA; EYE; FEMALE; GENETIC POLYMORPHISM; GENETICS; HUMAN; LEBER HEREDITARY OPTIC NEUROPATHY; LEIGH DISEASE; MALE; MITOCHONDRIAL GENE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; POINT MUTATION; PRESCHOOL CHILD;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; ANIMALS; ASIAN CONTINENTAL ANCESTRY GROUP; BASE SEQUENCE; BRAIN; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DYSTONIA; ELECTRON TRANSPORT COMPLEX I; EYE; FEMALE; GENES, MITOCHONDRIAL; HUMANS; LEIGH DISEASE; MALE; MOLECULAR SEQUENCE DATA; OPTIC ATROPHY, HEREDITARY, LEBER; PEDIGREE; POINT MUTATION; POLYMORPHISM, GENETIC; YOUNG ADULT;

EID: 79958158129     PISSN: 13646745     EISSN: 13646753     Source Type: Journal    
DOI: 10.1007/s10048-009-0194-0     Document Type: Article

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