Mroczek, M. Et Al. 2022. FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. JOURNAL OF MEDICAL GENETICS , vol.59, no.11 , 1069-1074.

Mroczek, M., Longman, C., Farrugia, M. E., Garcia, S. K., ARDIÇLI, D., Topaloglu, H., ... Hernandez-Lain, A.(2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. JOURNAL OF MEDICAL GENETICS , vol.59, no.11, 1069-1074.

Mroczek, Magdalena Et Al. "FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum," JOURNAL OF MEDICAL GENETICS , vol.59, no.11, 1069-1074, 2022

Mroczek, Magdalena Et Al. "FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum." JOURNAL OF MEDICAL GENETICS , vol.59, no.11, pp.1069-1074, 2022

Mroczek, M. Et Al. (2022) . "FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum." JOURNAL OF MEDICAL GENETICS , vol.59, no.11, pp.1069-1074.

@article{article, author={Magdalena Mroczek Et Al. }, title={FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum}, journal={JOURNAL OF MEDICAL GENETICS}, year=2022, pages={1069-1074} }