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2 min read

Last Updated: 8 August 2024

FGG Gene

The FGG gene encodes the gamma component of fibrinogen, a critical protein in blood clotting. Mutations in the FGG gene can lead to bleeding disorders, such as congenital afibrinogenaemia. Located on chromosome 4q31.3, the FGG gene plays a vital role in maintaining haemostasis and normal wound healing processes.

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