Cite
HARVARD Citation
Schweitzer, G. et al. (2019). A mutation in Site‐1 Protease is associated with a complex phenotype that includes episodic hyperCKemia and focal myoedema. Molecular genetics & genomic medicine. 7 (7), p. n/a. [Online].
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Schweitzer, G. et al. (2019). A mutation in Site‐1 Protease is associated with a complex phenotype that includes episodic hyperCKemia and focal myoedema. Molecular genetics & genomic medicine. 7 (7), p. n/a. [Online].