Sodium taurocholate cotransporter polypeptide deficiency with α-Thalassemia and Coffin-Siris syndrome
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Abstract
NTCPD, α-Thalassemia and CSS are three hereditary diseases associated with autosome. Especially, NTCPD and CSS are rarely reported in children. However, the co-occurrence of the three hereditary diseases occurred in a child, and presented complex and diverse genotypes and phenotypes, which has never been described.
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- last seen: 2026-05-19T01:45:01.086888+00:00