Deficiency of the voltage-dependent anion channel: A novel cause of mitochondriopathy

Pediatric Research

Volumn 39, Issue 5, 1996, Pages 760-765

  Huizing, Marjan ^a   Ruitenbeek, Wim ^a   Thinnes, Friedrich P ^b   DePinto, Vito ^c   Wendel, Udo ^a   Trijbels, Frans J M ^a   Smit, Leo M E ^d   Ter Laak, Henk J ^a   Van Den Heuvel, Lambert P ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b MAX PLANCK INSTITUTE OF EXPERIMENTAL MEDICINE   (Germany)

^c UNIVERSITY OF CATANIA   (Italy)

^d VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE NUCLEOTIDE TRANSLOCASE; ADENOSINE TRIPHOSPHATE; ANION CHANNEL; CARBONYL CYANIDE CHLOROPHENYLHYDRAZONE; MITOCHONDRIAL ENZYME; PYRUVIC ACID; VOLTAGE GATED CHANNEL FORMING PROTEIN;

ARTICLE; CASE REPORT; CHILD; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; FACE DYSMORPHIA; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; MEMBRANE POTENTIAL; MITOCHONDRIAL MEMBRANE; PRIORITY JOURNAL; PSYCHOMOTOR RETARDATION; SKIN FIBROBLAST;

EID: 0029914301     PISSN: 00313998     EISSN: None     Source Type: Journal    
DOI: 10.1203/00006450-199605000-00003     Document Type: Article

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