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Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.
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Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies.
Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies. Brain. 2007 Aug; 130(Pt 8):2024-36.
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PubMed
subject areas
Adult
Amino Acid Sequence
Child
Female
Humans
Magnetic Resonance Imaging
Male
Molecular Sequence Data
Muscle, Skeletal
Mutation
Myopathies, Structural, Congenital
Phenotype
Ryanodine Receptor Calcium Release Channel
Sequence Alignment
authors with profiles
Michael R Rose