Molecular pathogenetic mechanism of maternally inherited deafness

Annals of the New York Academy of Sciences

Volumn 1011, Issue , 2004, Pages 259-271

  Guan, Min Xin ^a,b  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Deafness; Maternally inherited deafness; Mitochondrial DNA; Mutations

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT; MITOCHONDRIAL DNA; TRANSFER RNA;

CLINICAL FEATURE; CONFERENCE PAPER; DISEASE ASSOCIATION; DNA REPLICATION; DRUG CYTOTOXICITY; ENVIRONMENTAL FACTOR; EXTRACHROMOSOMAL INHERITANCE; GENE INSERTION; GENE MUTATION; GENETIC LINKAGE; HAPLOTYPE; HEARING LOSS; HETEROPLASMY; HOMOPLASY; HUMAN; KEARNS SAYRE SYNDROME; MATERNALLY INHERITED DIABETES AND DEAFNESS; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL GENETICS; MORPHOLOGICAL TRAIT; OTOTOXICITY; OXIDATIVE PHOSPHORYLATION; PATHOGENICITY; PERCEPTION DEAFNESS; POINT MUTATION; RNA GENE;

INSERTION SEQUENCES;

EID: 1842678661     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1196/annals.1293.025     Document Type: Conference Paper

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