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

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The defining pathology of the new clinical and histopathologic

The Digestive System

Variants of the ACTG2 gene correlate with degree of severity and

Compound heterozygous variants in MYH11 underlie autosomal

Megacystis-microcolon-intestinal hypoperistalsis syndrome

PDF) Diagnostic Criteria of Pediatric Intestinal Myopathies

Multisystem smooth muscle dysfunction syndrome in a Chinese girl

Multisystem smooth muscle dysfunction syndrome in a Chinese girl

Heterozygous De Novo and Inherited Mutations in the Smooth Muscle

Visceral myopathy diagnosed by a de novo ACTG2 mutation in a

The Digestive System

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