Non-syndromic deafness associated with a mutation and a polymorphism in the mitochondrial 12S ribosomal RNA gene in a large Zairean pedigree

European Journal of Human Genetics

Volumn 4, Issue 1, 1996, Pages 46-51

  Matthijs, Gert ^a  

^a UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

12S ribosomal RNA; Aminoglycosides; Hereditary deafness; Mitochondrial DNA; Mutation; Polymorphism

Indexed keywords

MITOCHONDRIAL RNA; RIBOSOME RNA;

ARTICLE; CLINICAL ARTICLE; DEMOCRATIC REPUBLIC CONGO; FEMALE; GENETIC POLYMORPHISM; HEARING IMPAIRMENT; HUMAN; MALE; MUTANT; PEDIGREE; POINT MUTATION; PRIORITY JOURNAL; RNA GENE;

HUMAN HERPESVIRUS 4;

EID: 0029916599     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1159/000472169     Document Type: Article

References (1)

1. Gold M, Rapin I: Non-Mendelian mitochondrial inheritance as a cause of progressive genetic sensorineural hearing loss. Int J Pediatr Otorhinolaryngol 1994;30:91-104.