Neonatal jaundice caused by compound mutations of SLC10A1 and a novel UGT1A1 gene - 13/04/24
Doi : 10.1016/j.clinre.2024.102340
Meifen Wang a, 1, Tao Chen b, 1, Rui Chen a, Zhongrui Bi a, Junchao Peng a, Qi Shao a, Jiwei Li c, ⁎ 
a Department of Infectious Diseases, Kunming Children’s Hospital, The Affiliated Children’s Hospital of Kunming Medical University; Yunnan Province Clinical Research Center for Children’s Health and Disease, Kunming, PR China
b Department of Stomatology, The Affiliated Hospital of Yunnan Normal University, Kunming, PR China
c Department of Pathology, Kunming Children's Hospital, The Affiliated Children's Hospital of Kunming Medical University; Yunnan Province Clinical Research Center for Children's Health and Disease, Kunming, PR China
⁎Corresponding author at: Kunming Children's Hospital, The Affiliated Children's Hospital of Kunming Medical University, Kunming 650228, PR China.Kunming Children's HospitalThe Affiliated Children's Hospital of Kunming Medical UniversityKunming650228PR China
Keywords : Neonatal jaundice, NTCPD, SLC10A1 gene, UGT1A1 gene
Abbreviations : NTCPD, SLC10A1, OATP, UGT1A1, TBIL, DBIL, IBIL, TBA, ALP, VD, GS, CN-I, CN-II
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© 2024
Pubblicato da Elsevier Masson SAS.
Vol 48 - N° 5
Articolo 102340- Maggio 2024 Ritorno al numero
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