Tyro3 Modulates Mertk-Associated Retinal Degeneration
Tyro3 Modulates Mertk-Associated Retinal Degeneration
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United States: Public Library of Science
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Language
English
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United States: Public Library of Science
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Contents
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 murine genetic modifier of Mertk-associated photorec...
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Full title
Tyro3 Modulates Mertk-Associated Retinal Degeneration
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TN_cdi_plos_journals_1764369614
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1764369614
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ISSN
1553-7404,1553-7390
E-ISSN
1553-7404
DOI
10.1371/journal.pgen.1005723
