Cite
HARVARD Citation
Hanley, A. et al. (2016). Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. BMC medical genetics. 17 (1), pp. 1-7. [Online].
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Hanley, A. et al. (2016). Mutation of a common amino acid in NKX2.5 results in dilated cardiomyopathy in two large families. BMC medical genetics. 17 (1), pp. 1-7. [Online].