Increased steroidogenesis promotes early-onset and severe vision loss in females with OPA1 dominant optic atrophy.

Sarzi, Emmanuelle; Seveno, Marie; Angebault, Claire; Milea, Dan; Rönnbäck, Cecilia; Quilès, Melanie; Adrian, Mathias; Grenier, Joanna; Caignard, Angélique; Lacroux, Annie; Lavergne, Christian; Reynier, Pascal; Larsen, Michael; Hamel, Christian P; Delettre, Cécile; Lenaers, Guy; Müller, Agnès

Sarzi, Emmanuelle; Seveno, Marie; Angebault, Claire; Milea, Dan; Rönnbäck, Cecilia; Quilès, Melanie; Adrian, Mathias; Grenier, Joanna; Caignard, Angélique; Lacroux, Annie; Lavergne, Christian; Reynier, Pascal; Larsen, Michael; Hamel, Christian P; Delettre, Cécile; Lenaers, Guy; Müller, Agnès.

Afiliação

Sarzi E; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Seveno M; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Angebault C; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Milea D; Département de Biochimie et Génétique, UMR CNRS 6214-INSERM 1083, Centre Hospitalier Universitaire, Angers, France.
Rönnbäck C; Singapore National Eye Centre, Singapore.
Quilès M; Singapore Eye Research Institute, Singapore.
Adrian M; Duke-NUS, Singapore.
Grenier J; Department of Ophthalmology, Glostrup Hospital, Glostrup, Denmark.
Caignard A; Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Lacroux A; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Lavergne C; Université de Montpellier - Faculté de Pharmacie-Montpellier, France.
Reynier P; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Larsen M; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Hamel CP; Centre de référence des affections sensorielles d'origine génétique, Hôpital Gui de Chauliac, Montpellier, France.
Delettre C; Département de Biochimie et Génétique, UMR CNRS 6214-INSERM 1083, Centre Hospitalier Universitaire, Angers, France.
Lenaers G; INSERM U1051 - Institut des Neurosciences de Montpellier, Montpellier, France.
Müller A; Centre de référence des affections sensorielles d'origine génétique, Hôpital Gui de Chauliac, Montpellier, France.

Hum Mol Genet ; 26(23): 4764, 2017 12 01.

Article em En | MEDLINE | ID: mdl-29045675

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: França

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