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Congenital heart defect causing mutation in Nkx2.5 displays in vivo functional deficit
Zakariyah, Abeer F., Rajgara, Rashida F., Veinot, John P., Skerjanc, Ilona S., Burgon, Patrick G.Volume:
105
Language:
english
Journal:
Journal of Molecular and Cellular Cardiology
DOI:
10.1016/j.yjmcc.2017.03.003
Date:
April, 2017
File:
PDF, 1.37 MB
english, 2017