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] |
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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 proteins. Biomedicine & Pharmacotherapy 2024; 175: 116618 doi: 10.1016/j.biopha.2024.116618
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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 function. Journal of Endocrinological Investigation 2022; 45(4): 731 doi: 10.1007/s40618-021-01697-z
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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 Korea. Endocrinology and Metabolism 2022; 37(6): 870 doi: 10.3803/EnM.2022.1591
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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 Review. Diabetes, Metabolic Syndrome and Obesity 2023; : 2225 doi: 10.2147/DMSO.S413048
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5 |
Yanlan Fang, Hong Chen, Qingqing Chen, Chunlin Wang, Li Liang. Compound hemizygous variants in SERPINA7 gene cause thyroxine‐binding globulin deficiency. Molecular Genetics & Genomic Medicine 2021; 9(2) doi: 10.1002/mgg3.1571
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