Stargardt disease: clinical features, molecular genetics, animal models and therapeutic options

Stargardt disease (STGD1; MIM 248200) is the most prevalent inherited macular dystrophy and is associated with disease-causing sequence variants in the gene ABCA4. Significant advances have been made over the last 10 years in our understanding of both the clinical and molecular features of STGD1, an...

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Detalles Bibliográficos
Autores principales: Tanna, Preena, Strauss, Rupert W, Fujinami, Kaoru, Michaelides, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256119/
https://www.ncbi.nlm.nih.gov/pubmed/27491360
http://dx.doi.org/10.1136/bjophthalmol-2016-308823

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5256119/
https://www.ncbi.nlm.nih.gov/pubmed/27491360
http://dx.doi.org/10.1136/bjophthalmol-2016-308823

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