Inherited mitochondrial disorders

Advances in Experimental Medicine and Biology

Volumn 942, Issue , 2012, Pages 187-213

  Finsterer, Josef ^a  

^a DANUBE UNIVERSITY KREMS   (Austria)

Author keywords

Encephalomyopathy; Genetics; Metabolic disease; Mitochondrial DNA; Multisystem disease; Neuromuscular

Indexed keywords

MITOCHONDRIAL DNA;

ALPERS DISEASE; AMINOGLYCOSIDE INDUCED DEAFNESS; ARTICLE; BARTH SYNDROME; CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; DISORDERS OF MITOCHONDRIAL FUNCTIONS; EXTRACHROMOSOMAL INHERITANCE; GENE DELETION; GENE DUPLICATION; GENE LOCATION; GENETIC HETEROGENEITY; GENETIC SCREENING; GENETIC TRAIT; HEARING IMPAIRMENT; HUMAN; KEARNS SAYRE SYNDROME; LEBER HEREDITARY OPTIC NEUROPATHY; LEIGH DISEASE; MATERNALLY INHERITED DIABETES AND DEAFNESS; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL DNA DEPLETION SYNDROME; MITOCHONDRIAL DNA DISORDER; MITOCHONDRIAL GENE; MITOCHONDRIAL RESPIRATION; MNGIE SYNDROME; MUTATIONAL ANALYSIS; NARP SYNDROME; NONHUMAN; PATHOGENESIS; PEARSON SYNDROME; POINT MUTATION; PRIORITY JOURNAL; WOLFRAM SYNDROME; X LINKED SIDEROBLASTIC ANEMIA;

GENETIC DISEASES, INBORN; HUMANS; MITOCHONDRIAL DISEASES;

EID: 84859907325     PISSN: 00652598     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-94-007-2869-1_8     Document Type: Article

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