Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA.

Majamaa-Voltti, K; Turkka, J; Kortelainen, M-L; Huikuri, H; Majamaa, K

Majamaa-Voltti, K; Turkka, J; Kortelainen, M-L; Huikuri, H; Majamaa, K.

Affiliation

Majamaa-Voltti K; Department of Internal Medicine, University of Oulu, P.O. Box 5000, FIN-90014 Oulu, Finland. kirsi.majamaa-voltti@ppshp.fi

J Neurol Neurosurg Psychiatry ; 79(2): 209-11, 2008 Feb.

Article in En | MEDLINE | ID: mdl-18202211

Subject(s)

Adenine Nucleotides/genetics; Cause of Death; Guanine Nucleotides/genetics; Mitochondrial Diseases/mortality; Mitochondrial Proteins/genetics; Phenotype; RNA, Transfer, Amino Acyl/genetics; Adolescent; Adult; Base Sequence; Cardiomyopathies/genetics; Cardiomyopathies/mortality; Child; Child, Preschool; DNA Mutational Analysis; DNA, Mitochondrial/genetics; Death, Sudden/epidemiology; Diabetes Mellitus/genetics; Diabetes Mellitus/mortality; Female; Finland; Genetic Carrier Screening; Heart Failure/mortality; Humans; Infant; Infant, Newborn; Kaplan-Meier Estimate; Life Expectancy; Male; Mitochondrial Diseases/diagnosis; Mitochondrial Diseases/genetics; Nervous System Diseases/genetics; Nervous System Diseases/mortality; Status Epilepticus/genetics; Survival Analysis

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Full text: 1 Collection: 01-internacional Health context: 2_ODS3 / 6_ODS3_enfermedades_notrasmisibles Database: MEDLINE Main subject: Phenotype / RNA, Transfer, Amino Acyl / Adenine Nucleotides / Cause of Death / Mitochondrial Diseases / Mitochondrial Proteins / Guanine Nucleotides Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Aspects: Patient_preference Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Country/Region as subject: Europa Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2008 Document type: Article

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