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Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.
La Morgia, C; Achilli, A; Iommarini, L; Barboni, P; Pala, M; Olivieri, A; Zanna, C; Vidoni, S; Tonon, C; Lodi, R; Vetrugno, R; Mostacci, B; Liguori, R; Carroccia, R; Montagna, P; Rugolo, M; Torroni, A; Carelli, V.
Affiliation
  • La Morgia C; Dipartimento di Scienze Neurologiche, Università di Bologna, Via Ugo Foscolo 7, 40123 Bologna, Italy.
Neurology ; 70(10): 762-70, 2008 Mar 04.
Article in En | MEDLINE | ID: mdl-18216301
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Genetic Predisposition to Disease / Optic Atrophy, Hereditary, Leber / Energy Metabolism / Mutation / Myoclonus Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Italia Country of publication: Estados Unidos
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Genetic Predisposition to Disease / Optic Atrophy, Hereditary, Leber / Energy Metabolism / Mutation / Myoclonus Type of study: Prognostic_studies Limits: Adult / Female / Humans / Male / Middle aged Language: En Journal: Neurology Year: 2008 Document type: Article Affiliation country: Italia Country of publication: Estados Unidos