Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy

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Protein Cell ›› 2022, Vol. 13 ›› Issue (1) : 65-71. DOI: 10.1007/s13238-021-00843-w
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Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy

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