ana-ferreiro documents

Multi-minicore disease–searching for boundaries: Phenotype analysis of 38 cases
Documents Multi-minicore disease–searching for boundaries: Phenotype analysis of 38 cases
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
Documents 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