Sitosterolemia With Two Heterozygous Variants Including a Novel Mutation c.1800T&gt;A in the ABCG5 Gene: A Case Report of a Rare Condition in a Young Saudi Girl

Ali S. Alquraishi; Syed Rayees; Ali S. Alquraishi; Syed Rayees

doi:10.7759/cureus.63088

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