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Found 1 from your keywords: subject="SLC4A1"
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Southeast Asian Ovalocytosis (sao) Diagnosis Using Microscopy And Molecular D…
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Devin

Southeast Asian Ovalocytosis (SAO) is a hereditary genetic disorder caused by a 27 bp deletion in the SLC4A1 gene, leading to a disrupted folding at the extracellular face of the SLC4A1 protein in the red blood cell (RBC) membrane. SAO is an autosomal dominant disorder where heterozygous individuals are asymptomatic and homozygous SAO are considered embryonic lethal. SAO can be observed microsc…

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EP BM-006