A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium
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| Description | scientific article |
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author: Natalia Ronkina Guy Lenaers Matthias Gaestel Alain Gaudric |
| Publication date | January 6, 2016 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |