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Publications by Ali Rad
Two Patients With the Heterozygous R189H Mutation in ACTA2 and Complex Congenital Heart Defects Expands the Cardiac Phenotype of Multisystemic Smooth Muscle Dysfunction Syndrome
American Journal of Medical Genetics, Part A
Genetics
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Smooth Muscle Α Actin (Acta2) and Myofibroblast Function During Hepatic Wound Healing
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Multidisciplinary
