Cite
HARVARD Citation
Assia Batzir, N. et al. (2020). Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Human mutation. 41 (3), pp. 641-654. [Online].
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Assia Batzir, N. et al. (2020). Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Human mutation. 41 (3), pp. 641-654. [Online].