Cite
HARVARD Citation
Kaindl, A. et al. (2004). Missense mutations of ACTA1 cause dominant congenital myopathy with cores. Journal of medical genetics. 41 (11), pp. 842-848. [Online].
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Kaindl, A. et al. (2004). Missense mutations of ACTA1 cause dominant congenital myopathy with cores. Journal of medical genetics. 41 (11), pp. 842-848. [Online].