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Compound heterozygosity deteriorates phenotypes of hypertrophic cardiomyopathy with founder MYBPC3 mutation: evidence from patients and zebrafish models
Hodatsu, A., Konno, T., Hayashi, K., Funada, A., Fujita, T., Nagata, Y., Fujino, N., Kawashiri, M.-a., Yamagishi, M.Volume:
307
Language:
english
Journal:
AJP: Heart and Circulatory Physiology
DOI:
10.1152/ajpheart.00637.2013
Date:
December, 2014
File:
PDF, 1.49 MB
english, 2014