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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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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    Isabelle Meunier
    Béatrice Bocquet
    Corinne Baudoin
    Camille Piro-Megy
    Aurélie Cubizolle
    Mélanie Quilès
    Albert Jean-Charles
    Salomon Yves Cohen
    Harold Merle
    Gilles Labesse
    Gaël Manes
    Marie Péquignot
    Chantal Cazevieille
    Claire-Marie Dhaenens
    Agnès Fichard
    Simon J Arthur
    Christian P Hamel
    6 January 2016
    916-926

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