Mitochondrial defects and hearing loss.

Hutchin, T P; Cortopassi, G A

Hutchin, T P; Cortopassi, G A.

Affiliation

Hutchin TP; Molecular Medicine Unit, University of Leeds, St James's University Hospital, United Kingdom. t.p.hutchin@leeds.ac.uk

Cell Mol Life Sci ; 57(13-14): 1927-37, 2000 Dec.

Article in En | MEDLINE | ID: mdl-11215518

Subject(s)

Deafness/genetics; Deafness/pathology; Mitochondrial Myopathies/genetics; Mitochondrial Myopathies/pathology; Aminoglycosides/toxicity; Cell Nucleus/genetics; Cochlea/metabolism; Cochlea/pathology; DNA, Mitochondrial/genetics; Deafness/therapy; Genetic Counseling; Humans; Mitochondrial Myopathies/therapy; Models, Biological; Mutation; RNA, Ribosomal/genetics; RNA, Transfer, Leu/genetics; RNA, Transfer, Ser/genetics; Syndrome

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PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Mitochondrial Myopathies / Deafness Limits: Humans Language: En Journal: Cell Mol Life Sci Year: 2000 Document type: Article

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