Genetic Spectrum of ABCA4-Associated Retinal Degeneration in Poland

Mutations in retina-specific ATP-binding cassette transporter 4 (ABCA4) are responsible for over 95% of cases of Stargardt disease (STGD), as well as a minor proportion of retinitis pigmentosa (RP) and cone-rod dystrophy cases (CRD). Since the knowledge of the genetic causes of inherited retinal dis...

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Detalles Bibliográficos
Autores principales: Tracewska, Anna M., Kocyła-Karczmarewicz, Beata, Rafalska, Agnieszka, Murawska, Joanna, Jakubaszko-Jablonska, Joanna, Rydzanicz, Małgorzata, Stawiński, Piotr, Ciara, Elżbieta, Khan, Muhammad Imran, Henkes, Arjen, Hoischen, Alexander, Gilissen, Christian, van de Vorst, Maartje, Cremers, Frans P. M., Płoski, Rafał, Chrzanowska, Krystyna H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947411/
https://www.ncbi.nlm.nih.gov/pubmed/31766579
http://dx.doi.org/10.3390/genes10120959

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947411/
https://www.ncbi.nlm.nih.gov/pubmed/31766579
http://dx.doi.org/10.3390/genes10120959

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