Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Thyrotoxicosis and SCN4A[original query] |
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Absence of ion channels CACN1AS and SCN4A mutations in thyrotoxic hypokalemic periodic paralysis. Thyroid : official journal of the American Thyroid Association 2004 Mar 14 (3): 187-90. Ng WY, Lui KF, Thai AC, Cheah JS |
Thyrotoxic periodic paralysis associated with a mutation in the sodium channel gene SCN4A. Journal of pediatric endocrinology & metabolism : JPEM 2005 1 17 (12): 1679-82. Lane Andrew H, Markarian Katherine, Braziunene Ie |
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