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La PKAD est secondaire à une mutation du gène PKD2 dans près de 20 % des cas. Nous proposons de décrire précisemment les aspects cliniques, génétiques et pronostiques de la PKAD par mutation du gène PKD2.L’ensemble des 200 patients (135 familles) de la cohorte Genkyst présentant une mutation du gène PKD2 ont été inclus. L’influence des facteurs cliniques et génétiques a été étudiée par le modèle de...
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