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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Главные авторы: Douglas Vollrath, Douglas Yasumura, Gillie Benchorin, Michael T Matthes, Wei Feng, Natalie M Nguyen, Cecilia D Sedano, Melissa A Calton, Matthew M LaVail
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science (PLoS) 2015-12-01
Серии:PLoS Genetics
Online-ссылка:http://europepmc.org/articles/PMC4687644?pdf=render
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