Cite
HARVARD Citation
Bernal, S. et al. (2010). The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor. Journal of medical genetics. 47 (9), pp. 640-642. [Online].
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Bernal, S. et al. (2010). The c.859G>C variant in the SMN2 gene is associated with types II and III SMA and originates from a common ancestor. Journal of medical genetics. 47 (9), pp. 640-642. [Online].