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Cited by in CrossRef
For: Dang PP, Xiao WW, Shan ZY, Xi Y, Wang RR, Yu XH, Teng WP, Teng XC. Novel frameshift mutation causes early termination of the thyroxine-binding globulin protein and complete thyroxine-binding globulin deficiency in a Chinese family: A case report. World J Clin Cases 2019; 7(22): 3887-3894 [PMID: 31799319 DOI: 10.12998/wjcc.v7.i22.3887]
URL: https://www.wjgnet.com/2307-8960/full/v7/i22/3887.htm
Number Citing Articles
1
Sabina Janciauskiene, Urszula Lechowicz, Magdalena Pelc, Beata Olejnicka, Joanna Chorostowska-Wynimko. Diagnostic and therapeutic value of human serpin family proteinsBiomedicine & Pharmacotherapy 2024; 175: 116618 doi: 10.1016/j.biopha.2024.116618
2
S. Gawandi, K. Jothivel, S. Kulkarni. Identification of a novel mutation in thyroxine-binding globulin (TBG) gene associated with TBG-deficiency and its effect on the thyroid functionJournal of Endocrinological Investigation 2022; 45(4): 731 doi: 10.1007/s40618-021-01697-z
3
Jung Heo, Sang-Mi Kim, Hyun Jin Ryu, Hyunju Park, Tae Hyuk Kim, Jae Hoon Chung, Hyung-Doo Park, Sun Wook Kim. Identification of Mutations in the Thyroxine-Binding Globulin (TBG) Gene in Patients with TBG Deficiency in KoreaEndocrinology and Metabolism 2022; 37(6): 870 doi: 10.3803/EnM.2022.1591
4
Xuefang Liu, Suyan Li, Jingni Xiong, Dandan Chen, Chan Jiang, Liankun Zeng, Youyan Qiu, Bi-Wen Xia. Partial Thyroid Hormone-Binding Globulin Deficiency: A Case Report and Literature ReviewDiabetes, Metabolic Syndrome and Obesity 2023; : 2225 doi: 10.2147/DMSO.S413048
5
Yanlan Fang, Hong Chen, Qingqing Chen, Chunlin Wang, Li Liang. Compound hemizygous variants in SERPINA7 gene cause thyroxine‐binding globulin deficiencyMolecular Genetics & Genomic Medicine 2021; 9(2) doi: 10.1002/mgg3.1571