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2022
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2021
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2014
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Clinical and molecular characterization of mitochondrial DNA disorders in a group of Argentinian pediatric patients.
Not available
S-EPMC7933530
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biostudies-literature
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Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies.
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S-EPMC9271256
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biostudies-literature
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Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.
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S-EPMC4200603
|
biostudies-literature
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