Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations

PURPOSE: Sixteen different mutations in the guanylate cyclase activator 1A gene (GUCA1A), have been previously identified to cause autosomal dominant cone dystrophy (adCOD), cone–rod dystrophy (adCORD), macular dystrophy (adMD), and in an isolated patient, retinitis pigmentosa (RP). The purpose of t...

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Detalles Bibliográficos
Autores principales: Manes, Gaël, Mamouni, Sonia, Hérald, Emilie, Richard, Anne-Claire, Sénéchal, Audrey, Aouad, Karim, Bocquet, Béatrice, Meunier, Isabelle, Hamel, Christian P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389339/
https://www.ncbi.nlm.nih.gov/pubmed/28442884

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389339/
https://www.ncbi.nlm.nih.gov/pubmed/28442884

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