Not only dominant, not only optic atrophy: expanding the clinical spectrum associated with OPA1 mutations

BACKGROUND: Heterozygous mutations in OPA1 are a common cause of autosomal dominant optic atrophy, sometimes associated with extra-ocular manifestations. Few cases harboring compound heterozygous OPA1 mutations have been described manifesting complex neurodegenerative disorders in addition to optic...

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Detalles Bibliográficos
Autores principales: Nasca, Alessia, Rizza, Teresa, Doimo, Mara, Legati, Andrea, Ciolfi, Andrea, Diodato, Daria, Calderan, Cristina, Carrara, Gianfranco, Lamantea, Eleonora, Aiello, Chiara, Di Nottia, Michela, Niceta, Marcello, Lamperti, Costanza, Ardissone, Anna, Bianchi-Marzoli, Stefania, Iarossi, Giancarlo, Bertini, Enrico, Moroni, Isabella, Tartaglia, Marco, Salviati, Leonardo, Carrozzo, Rosalba, Ghezzi, Daniele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427524/
https://www.ncbi.nlm.nih.gov/pubmed/28494813
http://dx.doi.org/10.1186/s13023-017-0641-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5427524/
https://www.ncbi.nlm.nih.gov/pubmed/28494813
http://dx.doi.org/10.1186/s13023-017-0641-1

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