Cite
HARVARD Citation
Géraud, J. et al. (2021). Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy. Journal of medical genetics. 58 (9), pp. 602-608. [Online].
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Géraud, J. et al. (2021). Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy. Journal of medical genetics. 58 (9), pp. 602-608. [Online].