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Carron, J. et al. (n.d.). 54 Novel formin homology 2 domain containing 3 (FHOD3) mutations associated with the pathogenesis of hypertrophic cardiomyopathy (HCM) in an irish population. Heart. p. A43. [Online].
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Carron, J. et al. (n.d.). 54 Novel formin homology 2 domain containing 3 (FHOD3) mutations associated with the pathogenesis of hypertrophic cardiomyopathy (HCM) in an irish population. Heart. p. A43. [Online].