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If evening routines are quieter for you, managing side effects could be less intrusive on your daily life
Genetic Basis and Pathophysiology Most cases of MH are associated with mutations in the RYR1 gene , which encodes the ryanodine receptor type 1 (RyR1) calcium-release channel in skeletal muscle
Additionally, 30% of participants had severe depression
Mohammedi K, Woodward M, Marre M, Colgiuri S, Cooper M, Harrap S, Mancia G, Poulter N, Williams B, Zoungas S, Chalmers J
10.1038/srep10211 142 TurtonM
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