Human deafness dystonia syndrome is a mitochondrial disease

Proceedings of the National Academy of Sciences of the United States of America

Volumn 96, Issue 5, 1999, Pages 2141-2146

  Koehler, Carla M ^a   Leuenberger, Danielle ^a   Merchant, Sabeeha ^a,b   Renold, Anja ^a   Junne, Tina ^a   Schatz, Gottfried ^a  

^a UNIVERSITY OF BASEL   (Switzerland)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; CELL PROTEIN;

ANIMAL CELL; ARTICLE; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DYSTONIA; GENE MUTATION; HEARING IMPAIRMENT; INTRACELLULAR TRANSPORT; METABOLITE; NONHUMAN; PRIORITY JOURNAL; PROTEIN TRANSPORT;

AMINO ACID SEQUENCE; CARRIER PROTEINS; DEAFNESS; DNA-BINDING PROTEINS; DYSTONIA; ESCHERICHIA COLI PROTEINS; FUNGAL PROTEINS; HUMANS; INTRACELLULAR MEMBRANES; MEMBRANE TRANSPORT PROTEINS; MITOCHONDRIA; MITOCHONDRIAL MYOPATHIES; MOLECULAR SEQUENCE DATA; PROTEIN BIOSYNTHESIS; PROTEINS; RECOMBINANT PROTEINS; SACCHAROMYCES CEREVISIAE; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID; SUBMITOCHONDRIAL PARTICLES; SYNDROME;

ANIMALIA;

EID: 0033514928     PISSN: 00278424     EISSN: None     Source Type: Journal    
DOI: 10.1073/pnas.96.5.2141     Document Type: Article

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