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Compound heterozygous mutations in the SPTA1 gene. (A) Family tree of a Chinese family with a neonate with hereditary spherocytosis. Square and circle denote male and female, respectively. (B) SPTA1 c.3897-1G>C maternally transmitted mutation. (C) SPTA1 c.5029G>A paternally transmitted mutation. SPTA1, spectrin-α, erythrocytic 1.
