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MAPKAPK3 gene
Known as:
3PK
, MITOGEN-ACTIVATED PROTEIN KINASE-ACTIVATED PROTEIN KINASE 3
, MAPKAP3
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National Institutes of Health
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MAP-kinase-activated kinase 3
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2016
2016
A dominant mutation in MAPKAPK3, an actor of p38 signaling pathway, causes a new retinal dystrophy involving Bruch's membrane and retinal pigment epithelium.
I. Meunier
,
G. Lenaers
,
+18 authors
C. Hamel
Human Molecular Genetics
2016
Corpus ID: 22142893
Inherited retinal dystrophies are clinically and genetically heterogeneous with significant number of cases remaining genetically…
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