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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: 47 patients with FLNA associated periventricular nodular heterotopia

Fig. 1

a Patient age at onset of the seizure disorder (red) and at genetic diagnosis (blue) with diagnostic latency (black line); b schematic structure of the corresponding Filamin A protein (not to scale) with the two NH2-terminal actin binding calponin homology domains (CHD1-2) and 24 immunoglobulin-like filamin repeat domains interrupted by two hinge regions (red triangles)

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