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

$ 9.00

4.5
(95)
In stock
Description

MEGACYSTIS-MICROCOLON-INTESTINAL HYPOPERISTALSIS SYNDROME

What is ACTA2 Gene Mutations ∙ ACTA2 Alliance ∙ Foundation for

PDF) Diagnostic Criteria of Pediatric Intestinal Myopathies

PDF) Irregular bladder smooth muscle actin-gamma2 expression in

Quantitative analysis of V5 antibody-and phalloidin-stained HISMCs

ACTG2 Gene - GeneCards, ACTH Protein

Multisystem smooth muscle dysfunction syndrome in a Chinese girl

/plosgenetics/article/figure/imag

Kindlin-2 deficiency induces fatal intestinal obstruction in mice

ACTG2-Associated Visceral Myopathy With Chronic Intestinal

Visceral myopathy diagnosed by a de novo ACTG2 mutation in a

PDF) Prenatal diagnostic and management of megacystis microcolon

Smooth muscle actin isoforms: A tug of war between contraction and

Heterozygous De Novo and Inherited Mutations in the Smooth Muscle

The Digestive System