Retinitis pigmentosa and progressive sensorineural hearing loss caused by a C12258A mutation in the mitochondrial MTTS2 gene

American Journal of Human Genetics

Volumn 64, Issue 4, 1999, Pages 971-985

  Mansergh, Fiona C ^a   Millington Ward, Sophia ^a   Kennan, Avril ^a   Kiang, Anna Sophia ^a   Humphries, Marian ^a   Farrar, G Jane ^a   Humphries, Peter ^a   Kenna, Paul F ^a,b  

^a TRINITY COLLEGE DUBLIN   (Ireland)

^b Dept Otolaryngol Hd Neck Surg   (Ireland)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 9Q; CONTROLLED STUDY; GENE LOCUS; GENE MUTATION; GENETIC CONSERVATION; HUMAN; IRELAND; MAJOR CLINICAL STUDY; NONHUMAN; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RETINITIS PIGMENTOSA; USHER SYNDROME;

HOMO SAPIENS;

EID: 0033365294     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302344     Document Type: Article

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