Irregular bladder smooth muscle actin-gamma 2 expression in ACTG2 mutation-associated Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIHS): A case report

ACTG2-Associated Visceral Myopathy With Chronic Intestinal

Quantitative analysis of V5 antibody-and phalloidin-stained HISMCs

Compound heterozygous variants in MYH11 underlie autosomal

PDF) Extremely severe hypochloremic metabolic alkalosis after

What is ACTA2 Gene Mutations ∙ ACTA2 Alliance ∙ Foundation for

ACTG2 Gene - GeneCards, ACTH Protein

ACTG2 Gene - GeneCards, ACTH Protein

Heterozygous De Novo and Inherited Mutations in the Smooth Muscle

Variants of the ACTG2 gene correlate with degree of severity and

What is ACTA2 Gene Mutations ∙ ACTA2 Alliance ∙ Foundation for