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tpm3 protein, human
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A cutaneous epithelioid vascular tumor harboring a TPM3::ALK fusion.
Myopathy-causing mutation R91P in the TPM3 gene drastically impairs structural and functional proper…
Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy.
Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia.
Transcript-Based Diagnosis and Expanded Phenotype of an Intronic Mutation in TPM3 Myopathy.
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Molecular and Genetic Studies of Congenital Myopathies
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