A recessive form of central core disease, transiently presenting as multi-minicore disease, is associated with a homozygous mutation in the ryanodine receptor type 1 gene
Ferreiro A, Monnier N, Romero NB, et al.
Annals of neurology, 2002, 51, 6, p 750
Annals of neurology, 2002, 51, 6, p 750
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