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Fig. 4 | BMC Medical Genomics

Fig. 4

From: Novel compound heterozygous variants of the SEC23A gene in a Chinese family with cranio-lenticulo-sutural dysplasia based on data from a large cohort of congenital cataract patients

Fig. 4

Electron microscopy micrographs of cultured fibroblasts. Fibroblasts from the patient carrying compound heterozygous SEC23A gene variants had dilated ER (black arrows) (A). The unaffected father (B) and mother (C) carrying heterozygous SEC23A variants had normal endoplasmic reticulum (white arrows)

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BMC Medical Genomics

ISSN: 1755-8794

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