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HARVARD Citation
Marttila, M. et al. (n.d.). Mutation Update and Genotype–Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies. Human mutation. 35 (7), pp. 779-790. [Online].
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Marttila, M. et al. (n.d.). Mutation Update and Genotype–Phenotype Correlations of Novel and Previously Described Mutations in TPM2 and TPM3 Causing Congenital Myopathies. Human mutation. 35 (7), pp. 779-790. [Online].