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Department of General Surgery, Tangdu Hospital, Air Force Medical University, Xi’an, Shaanxi, People’s Republic of China
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.141), which mainly metabolizes prostaglandin E2 (PGE2). Solute carrier organic anion transporter family member 2A1 ( SLCO2A1 , MIM 601460) gene has also been shown to be associated with PHO ( 4 ). Mutations in HPGD or SLCO2A1 result in loss of metabolizing
Musculoskeletal Research Laboratory and Bone Quality and Health Assessment Centre, Department of Orthopedics & Traumatology, The Chinese University of Hong Kong, Hong Kong SAR, Hong Kong
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Department of Endocrinology, The First Affiliated Hospital of Shanxi Medical University, Taiyuan, Shanxi, China
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transporter family, member 2A1 ( SLCO2A1 ; MIM 601460), which encodes a prostaglandin transporter ( 1 , 5 ). The pathogenesis and inherited pattern were controversial for a long time until the year 2008, and Uppal et al. identified the mutation of HPGD as