A novel mitochondrial heteroplasmic C13806A point mutation associated with Iranian Friedreich's Ataxia

Cellular and Molecular Neurobiology

Volumn 29, Issue 2, 2009, Pages 225-233

  Heidari, Mohammad Mehdi ^a   Houshmand, Massoud ^b,c   Hosseinkhani, Saman ^a   Nafissi, Shahriar ^d   Scheiber Mojdehkar, Barbara ^e   Khatami, Mehri ^a  

^a TARBIAT MODARES UNIVERSITY   (Iran)

^b NATIONAL INSTITUTE OF GENETIC ENGINEERING AND BIOTECHNOLOGY   (Iran)

^c Special Medical Center Iran   (Iran)

^d UNIVERSITY OF TEHRAN   (Iran)

^e MEDICAL UNIVERSITY OF VIENNA   (Austria)

Author keywords

Friedreich's ataxia (FRDA); MtDNA; Mutation; NADH dehydrogenase (ND) genes; TTGE

Indexed keywords

DNA FRAGMENT; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE MARKER; DISEASE PREDISPOSITION; DNA POLYMORPHISM; ENVIRONMENTAL FACTOR; FEMALE; FRIEDREICH ATAXIA; GEL ELECTROPHORESIS; GENE IDENTIFICATION; HUMAN; IRAN; MALE; MITOCHONDRIAL GENOME; MITOCHONDRION; ONSET AGE; POINT MUTATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; RISK FACTOR; SCHOOL CHILD;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; ENERGY METABOLISM; FEMALE; FRIEDREICH ATAXIA; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; IRAN; MALE; NADH DEHYDROGENASE; POINT MUTATION; POLYMORPHISM, GENETIC; YOUNG ADULT;

EID: 60049091790     PISSN: 02724340     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10571-008-9315-9     Document Type: Article

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