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HARVARD Citation
Mroczek, M. et al. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of medical genetics. 59 (11), pp. 1069-1074. [Online].
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Mroczek, M. et al. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of medical genetics. 59 (11), pp. 1069-1074. [Online].