Disease: Cardiac valvular dysplasia- X-linked
- An integration-free iPSC line ZZUNEUi008-A derived from dermal fibroblasts of a child with cardiac valvular dysplasia carrying a mutation in FLNA gene
- Congenital valvular defects associated with deleterious mutations in the <em>PLD1</em> gene
- Congenital valvular defects associated with deleterious mutations in the PLD1 gene
- Developmental basis for filamin-A-associated myxomatous mitral valve disease
- Ehlers-Danlos syndrome with lethal cardiac valvular dystrophy in males carrying a novel splice mutation in FLNA
- FLNA Deficiency
- In-frame Variants in FLNA Proximal Rod 1 Domain Associate With a Predominant Cardiac Valvular Phenotype
- Longitudinal Echocardiographic Evaluation of an Unusual Presentation of X-Linked Myxomatous Valvular Dystrophy Caused by Filamin A Mutation
- Mitral valve regurgitation: use of the standard and the latest echocardiographic techniques for establishing the diagnosis
- Modulation of transforming growth factor-β signaling and extracellular matrix production in myxomatous mitral valves by angiotensin II receptor blockers
- On the diagnosis of congenital valvular heart diseases
- Sinus of Valsalva Aneurysm: A Potential Case of Filamin A Mutation
- Surgical experience for prolapse of both atrioventricular valves in a patient with filamin A mutation
- X-linked myxomatous valvular dystrophy in a patient with a novel mutation in the FLNA gene