Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy.
Li B, Zhan Y, Liang Q, Xu C, Zhou X, Cai H, Zheng Y, Guo Y, Wang L, Qiu W, Cui B, Lu C, Qian R, Zhou P, Chen H, Liu Y, Chen S, Li X, Sun N.
Li B, et al. Among authors: cui b.
Protein Cell. 2022 Jan;13(1):65-71. doi: 10.1007/s13238-021-00843-w. Epub 2021 Apr 22.
Protein Cell. 2022.
PMID: 33884582
Free PMC article.
No abstract available.