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Neuropatía óptica hereditaria y síndromes sistémicos asociados como resultado del solapamiento de 2 mutaciones mitocondriales / Hereditary optic neuropathy and systemic disease of the overlapping of two mitochondrial mutations
Gutiérrez-Ortiz, C; Rodrigo-Rey, S.
Affiliation
  • Gutiérrez-Ortiz, C; Hospital Universitario Príncipe de Asturias. Alcalá de Henares. España
  • Rodrigo-Rey, S; Hospital Universitario Príncipe de Asturias. Alcalá de Henares. España
Neurología (Barc., Ed. impr.) ; 36(6): 472-473, julio-agosto 2021. ilus, tab
Article in Spanish | IBECS | ID: ibc-219914
Responsible library: ES1.1
Localization: ES15.1 - BNCS
Subject(s)
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Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Ophthalmology / Lipomatosis, Multiple Symmetrical / DNA Mutational Analysis / Optic Nerve Diseases / Mitochondria Limits: Female / Humans Language: Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2021 Document type: Article Institution/Affiliation country: Hospital Universitario Príncipe de Asturias/España
Fulltext
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Full text: Available Collection: National databases / Spain Database: IBECS Main subject: Ophthalmology / Lipomatosis, Multiple Symmetrical / DNA Mutational Analysis / Optic Nerve Diseases / Mitochondria Limits: Female / Humans Language: Spanish Journal: Neurología (Barc., Ed. impr.) Year: 2021 Document type: Article Institution/Affiliation country: Hospital Universitario Príncipe de Asturias/España