Abnormal H-Tfam in a patient harboring a single mtDNA deletion.

Tessa, A; Manca, M L; Mancuso, M; Renna, M R; Murri, L; Martini, B; Santorelli, F M; Siciliano, G

Tessa, A; Manca, M L; Mancuso, M; Renna, M R; Murri, L; Martini, B; Santorelli, F M; Siciliano, G.

Affiliation

Tessa A; Department of Neurosciences, Institute of Neurology, University of Pisa.

Funct Neurol ; 15(4): 211-4, 2000.

Article in En | MEDLINE | ID: mdl-11213524

Subject(s)

DNA, Mitochondrial/genetics; DNA-Binding Proteins; Gene Deletion; Mitochondrial Proteins; Nuclear Proteins/genetics; Ophthalmoplegia, Chronic Progressive External/genetics; Ophthalmoplegia, Chronic Progressive External/physiopathology; Transcription Factors/genetics; Biopsy; Blotting, Southern/methods; DNA Primers/genetics; Female; Humans; Middle Aged; Muscle, Skeletal/pathology; Ophthalmoplegia, Chronic Progressive External/diagnosis; Point Mutation/genetics; Polymerase Chain Reaction

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Collection: 01-internacional Database: MEDLINE Main subject: Transcription Factors / DNA, Mitochondrial / Nuclear Proteins / Ophthalmoplegia, Chronic Progressive External / Gene Deletion / Mitochondrial Proteins / DNA-Binding Proteins Type of study: Diagnostic_studies Limits: Female / Humans / Middle aged Language: En Journal: Funct Neurol Journal subject: NEUROLOGIA Year: 2000 Document type: Article

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