Activity
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Arthrogryposis v3.67
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SCN4A
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Arina Puzriakova Phenotypes for gene: SCN4A were changed from Congenital Myasthenic Syndrome, Recessive; Hyperkalemic periodic paralysis, type 2, 170500 to Myasthenic syndrome, congenital, 16, OMIM:614198, Congenital myasthenic syndrome 16, MONDO:0013620
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Arthrogryposis v3.66
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SCN4A
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Arina Puzriakova commented on gene: SCN4A
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Arthrogryposis v3.11
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SCN4A
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Zornitza Stark reviewed gene: SCN4A: Rating: RED; Mode of pathogenicity: None; Publications: 26700687; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
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Arthrogryposis
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SCN4A
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Ellen McDonagh classified SCN4A as green
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Arthrogryposis
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SCN4A
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Ellen McDonagh commented on SCN4A
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Arthrogryposis
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SCN4A
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Alice Gardham marked SCN4A as ready
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Arthrogryposis
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SCN4A
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Alice Gardham classified SCN4A as red
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Arthrogryposis
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SCN4A
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Alice Gardham reviewed SCN4A
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