A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium (Q39248006)
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English | 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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A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium (English)
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Natalia Ronkina
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Isabelle Meunier
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Béatrice Bocquet
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Corinne Baudoin
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Camille Piro-Megy
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Aurélie Cubizolle
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Mélanie Quilès
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Albert Jean-Charles
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Salomon Yves Cohen
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Harold Merle
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Gilles Labesse
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Gaël Manes
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Marie Péquignot
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Chantal Cazevieille
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Claire-Marie Dhaenens
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Agnès Fichard
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Simon J Arthur
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Christian P Hamel
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6 January 2016
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