Cite
HARVARD Citation
Di Blasi, C. et al. (2015). A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia. Journal of medical genetics. 52 (9), pp. 617-626. [Online].
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Di Blasi, C. et al. (2015). A CASQ1 founder mutation in three Italian families with protein aggregate myopathy and hyperCKaemia. Journal of medical genetics. 52 (9), pp. 617-626. [Online].