Cite
HARVARD Citation
Carter, M. et al. (2019). Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. Channels. 13 (1), pp. 153-161. [Online].
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Carter, M. et al. (2019). Compound heterozygous CACNA1H mutations associated with severe congenital amyotrophy. Channels. 13 (1), pp. 153-161. [Online].