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High Mitochondrial DNA Copy Number Is a Protective Factor From Vision Loss in Heteroplasmic Leber's Hereditary Optic Neuropathy (LHON).
Bianco, Angelica; Bisceglia, Luigi; Russo, Luciana; Palese, Luigi L; D'Agruma, Leonardo; Emperador, Sonia; Montoya, Julio; Guerriero, Silvana; Petruzzella, Vittoria.
Affiliation
  • Bianco A; Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso - Università degli Studi Aldo Moro, Piazza G. Cesare, Bari, Italy.
  • Bisceglia L; Ospedale 'Casa Sollievo della Sofferenza' IRCCS, UOC Genetica Medica, San Giovanni Rotondo, Italy.
  • Russo L; Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso - Università degli Studi Aldo Moro, Piazza G. Cesare, Bari, Italy.
  • Palese LL; Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso - Università degli Studi Aldo Moro, Piazza G. Cesare, Bari, Italy.
  • D'Agruma L; Ospedale 'Casa Sollievo della Sofferenza' IRCCS, UOC Genetica Medica, San Giovanni Rotondo, Italy.
  • Emperador S; Departamento de Bioquímica, Biología Molecular y Celular; CIBERER, IIS-Aragón, Universidad de Zaragoza, Zaragoza, Spain.
  • Montoya J; Departamento de Bioquímica, Biología Molecular y Celular; CIBERER, IIS-Aragón, Universidad de Zaragoza, Zaragoza, Spain.
  • Guerriero S; Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso - Università degli Studi Aldo Moro, Piazza G. Cesare, Bari, Italy.
  • Petruzzella V; Dipartimento di Scienze Mediche di Base, Neuroscienze e Organi di Senso - Università degli Studi Aldo Moro, Piazza G. Cesare, Bari, Italy.
Invest Ophthalmol Vis Sci ; 58(4): 2193-2197, 2017 Apr 01.
Article in En | MEDLINE | ID: mdl-28403426
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Blindness / Optic Atrophy, Hereditary, Leber / Mitochondrial Diseases / DNA Copy Number Variations / Mitochondria / Mutation Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Invest Ophthalmol Vis Sci Year: 2017 Document type: Article Affiliation country: Italy Country of publication: United States
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Blindness / Optic Atrophy, Hereditary, Leber / Mitochondrial Diseases / DNA Copy Number Variations / Mitochondria / Mutation Type of study: Clinical_trials / Diagnostic_studies / Prognostic_studies Limits: Female / Humans / Male Language: En Journal: Invest Ophthalmol Vis Sci Year: 2017 Document type: Article Affiliation country: Italy Country of publication: United States