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FLNA gene

Discuss publications and research concerning the FLNA gene.

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Related literature

Hypoxia Modulates Nanovesicle Phenotype and Angiogenic Function From Human Pluripotent Stem Cells.
FLNA
A Novel In-Frame Deletion of FLNA in X-Linked Cardiac Valvular Dysplasia With Variable Clinical Spectrum.
FLNA
Epilepsies of presumed genetic etiology show enrichment of rare variants that occur in the general population.
FLNA
Targeted Next-Generation Sequencing of 406 Genes Identified Genetic Defects Underlying Congenital Heart Disease in Down Syndrome Patients.
FLNA
A novel truncating mutation in FLNA causes periventricular nodular heterotopia, Ehlers-Danlos-like collagenopathy and macrothrombocytopenia.
FLNA
Familial Ebstein Anomaly: Whole Exome Sequencing Identifies Novel Phenotype Associated With FLNA.
FLNA
Filamin A (FLNA) mutation-A newcomer to the childhood interstitial lung disease (ChILD) classification.
FLNA
Germline and somatic mutations in cortical malformations: Molecular defects in Argentinean patients with neuronal migration disorders.
FLNA
PINK1 and FLNA mutations association: A role for atypical parkinsonism?
FLNA
Lung disease associated with filamin A gene mutation: a case report.
FLNA

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