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UnknownMyofibrillar myopathies.
Not available
S-EPMC3052736 | biostudies-literature
UnknownCongenital myasthenic syndromes: pathogenesis, diagnosis, and treatment.
Not available
S-EPMC4520251 | biostudies-literature
UnknownWhat have we learned from the congenital myasthenic syndromes.
Not available
S-EPMC3050586 | biostudies-literature
UnknownNew horizons for congenital myasthenic syndromes.
Not available
S-EPMC3546605 | biostudies-literature
UnknownFurther observations in congenital myasthenic syndromes.
Not available
S-EPMC3478107 | biostudies-literature
UnknownReducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy.
Not available
S-EPMC3235356 | biostudies-literature
UnknownMutant SNAP25B causes myasthenia, cortical hyperexcitability, ataxia, and intellectual disability.
Not available
S-EPMC4277673 | biostudies-literature
UnknownCongenital myopathy associated with the triadin knockout syndrome.
Not available
S-EPMC5373784 | biostudies-literature
UnknownClinical and Pathologic Features of Congenital Myasthenic Syndromes Caused by 35 Genes-A Comprehensive Review.
Not available
S-EPMC9961056 | biostudies-literature
UnknownImpaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia.
Not available
S-EPMC4532561 | biostudies-literature
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