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Maladaptive innate immune training of myelopoiesis links inflammatory comorbidities
Keen 1 1 Centre for Metabolic Bone Disease, Royal National Orthopaedic Hospital, Stanmore, London, UK Objective: Hypophosphatasia (HPP) is a rare, genetic metabolic disorder characterized by reduced activity of serum alkaline phosphatase (ALP) and various symptoms from life-threatening, severely impaired mineralization at birth to musculoskeletal pain in adulthood
5 for a comparison of the primary sequence of human GPxs 14)
Miyazono K
Overview of Vitamin A - UpToDate (2025)
doi: 10.1002/glia.20433
