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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Shranjeno v:
Bibliografske podrobnosti
izdano v:PLoS Genet
Main Authors: Vollrath, Douglas, Yasumura, Douglas, Benchorin, Gillie, Matthes, Michael T., Feng, Wei, Nguyen, Natalie M., Sedano, Cecilia D., Calton, Melissa A., LaVail, Matthew M.
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2015
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4687644/
https://ncbi.nlm.nih.gov/pubmed/26656104
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1005723
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