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

HIGHLIGHTS

  • who: Bin Li from the Department Fudan University, Shanghai, China have published the research: Isogenic human pluripotent stem cell disease models reveal ABRA deficiency underlies cTnT mutation-induced familial dilated cardiomyopathy, in the Journal: (JOURNAL)

SUMMARY

    March 8, 2021 March @@

ACRONYMS

LAY DEFINITIONS

  • cardiomyopathy: A group of diseases in which the dominant feature is the involvement of the CARDIAC MUSCLE itself. Cardiomyopathies are classified according to their predominant pathophysiological features (DILATED CARDIOMYOPATHY; HYPERTROPHIC CARDIOMYOPATHY; RESTRICTIVE CARDIOMYOPATHY) or their etiological/pathological factors (CARDIOMYOPATHY, ALCOHOLIC; ENDOCARDIAL FIBROELASTOSIS)
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