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Description
Clinical significance of the SLC33A1 encoded transporter is evident from the fact that mutation in the gene are associated with a lethal disorder identified as Huppke-Brendel syndrome (HPBDS)
Children with CdLS have autistic features and mild to severe intellectual disability [385]
Schiffrin, E
Designed to replenish essential vitamins and minerals directly into the bloodstream, this treatment has gained a loyal following among those seeking to improve energy levels, immune function, and overall well-being
