Mitochondrial disorders due to nuclear OXPHOS gene defects

Advances in Experimental Medicine and Biology

Volumn 652, Issue , 2009, Pages 85-116

  Ugalde, Cristina ^a   Morán, María ^b   Blázquez, Alberto ^b   Arenas, Joaquín ^b   Martín, Miguel A ^b  

^a INSTITUTO DE SALUD CARLOS III   (Spain)

^b NONE

Author keywords

Mitochondrial biogenesis; Mitochondrial respiratory chain; Nuclear gene defect; OXPHOS disorders; Respiratory subunits assembly

Indexed keywords

BCS1L PROTEIN; CHROMOSOME PROTEIN; CYTOCHROME B; CYTOCHROME C OXIDASE; IRON SULFUR PROTEIN; MITOCHONDRIAL PROTEIN; NUCLEAR PROTEIN; PROTEIN C8ORF38; PROTEIN NDUFA1; PROTEIN NDUFS8; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE (UBIQUINONE); REGULATOR PROTEIN; SUCCINATE DEHYDROGENASE; SUCCINATE DEHYDROGENASE (UBIQUINONE); UBIDECARENONE; UBIQUINOL CYTOCHROME C REDUCTASE; UNCLASSIFIED DRUG;

BARTH SYNDROME; BCS1L GENE; BIOGENESIS; C8ORF38 GENE; CLINICAL FEATURE; COENZYME Q10 DEFICIENCY; COMPLEX I DEFICIENCY; COMPLEX II DEFICIENCY; COMPLEX III DEFICIENCY; COMPLEX V DEFICIENCY; CONFERENCE PAPER; CYTOCHROME B GENE; CYTOCHROME C OXIDASE DEFICIENCY; CYTOCHROME C OXIDASE GENE; DISEASE ASSOCIATION; ENZYME DEFICIENCY; GENE FUNCTION; GENETIC CODE; HUMAN; MISSENSE MUTATION; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL RESPIRATION; MOLECULAR DYNAMICS; MUTATIONAL ANALYSIS; MUTATOR GENE; NDUFA1 GENE; NDUFS8 GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATIVE PHOSPHORYLATION; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN ASSEMBLY; PROTEIN DEFECT; PROTEIN FUNCTION; PROTEIN SYNTHESIS; PROTEIN TRANSPORT; RNA TRANSLATION; STRUCTURAL GENE; SUCCINATE DEHYDROGENASE GENE; CELL NUCLEUS; DISORDERS OF MITOCHONDRIAL FUNCTIONS; GENETICS; MITOCHONDRION; MUTATION; REVIEW;

CELL NUCLEUS; HUMANS; MITOCHONDRIA; MITOCHONDRIAL DISEASES; MUTATION; OXIDATIVE PHOSPHORYLATION; PROTEIN BIOSYNTHESIS;

EID: 77950346575     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-90-481-2813-6_7     Document Type: Conference Paper

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