Hereditary myokymia type 1 is an autosomal dominant disorder characterized by spntaneous contractions of muscle fibers and hypomagnesemia.
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Glaudemans B et al. (2009) A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia. ![]() |
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OMIM.ORG article Omim 160120![]() |