A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13

American Journal of Human Genetics

Volumn 68, Issue 2, 2001, Pages 386-396

  Seyda, A ^a   Newbold, R F ^a   Hudson, T J ^a   Verner, A ^a   Mackay, N ^a   Winter, S ^a   Feigenbaum, A ^a   Malaney, S ^a   Gonzalez Halphen, D ^a   Cuthbert, A P ^a   Robinson, B H ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

2 OXOISOVALERATE DEHYDROGENASE (LIPOAMIDE); CYTOCHROME C OXIDASE; GLYCINE; ISOLEUCINE; LEUCINE; OXOGLUTARATE DEHYDROGENASE; PYRUVATE DEHYDROGENASE COMPLEX; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; SUCCINATE DEHYDROGENASE; UBIQUINOL CYTOCHROME C REDUCTASE; VALINE;

ANIMAL CELL; ARTICLE; CASE REPORT; CHROMOSOME 2P; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME ACTIVITY; ENZYME DEFICIENCY; FEMALE; FIBROBLAST; GENE MAPPING; HUMAN; HUMAN CELL; HUMAN TISSUE; HYBRID CELL; IMMUNOBLOTTING; MALE; NEWBORN; NONHUMAN; PRIORITY JOURNAL; URINALYSIS;

ANIMALIA;

EID: 0035121867     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/318196     Document Type: Article

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