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Deep sequencing of mitochondrial genomes reveals increased mutation load in Friedreich's ataxia.
Bhalla, Angela D; Khodadadi-Jamayran, Alireza; Li, Yanjie; Lynch, David R; Napierala, Marek.
Affiliation
  • Bhalla AD; Department of Biochemistry and Molecular Genetics University of Alabama at Birmingham UAB Stem Cell Institute 1825 University Blvd. Birmingham Alabama 35294.
  • Khodadadi-Jamayran A; Department of Biochemistry and Molecular Genetics University of Alabama at Birmingham UAB Stem Cell Institute 1825 University Blvd. Birmingham Alabama 35294.
  • Li Y; Department of Biochemistry and Molecular Genetics University of Alabama at Birmingham UAB Stem Cell Institute 1825 University Blvd. Birmingham Alabama 35294.
  • Lynch DR; Division of Neurology and Pediatrics Children's Hospital of Philadelphia Abramson Research Center Room 502 Philadelphia Pennsylvania 19104.
  • Napierala M; Department of Biochemistry and Molecular Genetics University of Alabama at Birmingham UAB Stem Cell Institute 1825 University Blvd. Birmingham Alabama 35294; Department of Molecular Biomedicine Institute of Bioorganic Chemistry Polish Academy of Sciences Poznan 61-704 Poland.
Ann Clin Transl Neurol ; 3(7): 523-36, 2016 07.
Article in En | MEDLINE | ID: mdl-27386501
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Clin Transl Neurol Year: 2016 Document type: Article Country of publication: Estados Unidos
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Ann Clin Transl Neurol Year: 2016 Document type: Article Country of publication: Estados Unidos