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  • Molecular assay reagents intended to identify mutations in the calcium channel, voltage-dependent, L type, alpha 1S subunit (CACNA1S), located at chromosome 1q32, which encodes for the alpha-1S subunit of L-type calcium channels that are involved in excitation-contraction coupling in skeletal muscle. Mutations at this locus have been identified in most patients with hyperkalemic periodic paralysis (HKPP) and malignant hyperthermia susceptibility 5 (MHS5).
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