Tyro3 Modulates Mertk-Associated Retinal Degeneration

Inherited photoreceptor degenerations (IPDs) are the most genetically heterogeneous of Mendelian diseases. Many IPDs exhibit substantial phenotypic variability, but the basis is usually unknown. Mutations in MERTK cause recessive IPD phenotypes associated with the RP38 locus. We have identified a mu...

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Detalles Bibliográficos
Autores principales: Vollrath, Douglas, Yasumura, Douglas, Benchorin, Gillie, Matthes, Michael T., Feng, Wei, Nguyen, Natalie M., Sedano, Cecilia D., Calton, Melissa A., LaVail, Matthew M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687644/
https://www.ncbi.nlm.nih.gov/pubmed/26656104
http://dx.doi.org/10.1371/journal.pgen.1005723

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4687644/
https://www.ncbi.nlm.nih.gov/pubmed/26656104
http://dx.doi.org/10.1371/journal.pgen.1005723

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