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Skeletal Muscle Channelopathies v1.27 KCNJ2 Arina Puzriakova Phenotypes for gene: KCNJ2 were changed from Hypokalemic Periodic Paralysis, Type 2; Episodic weakness; Periodic paralysis; ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS; Andersen syndrome to Andersen syndrome, OMIM:170390; Andersen-Tawil syndrome, MONDO:0008222; Episodic weakness; Periodic paralysis
Skeletal Muscle Channelopathies KCNJ2 Fowzan ALKURAYA reviewed KCNJ2
Skeletal Muscle Channelopathies KCNJ2 Arianna Tucci marked KCNJ2 as ready
Skeletal Muscle Channelopathies KCNJ2 Arianna Tucci commented on KCNJ2
Skeletal Muscle Channelopathies KCNJ2 Arianna Tucci reviewed KCNJ2