Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene
- PMID: 14974930
- DOI: 10.1046/j.1365-2265.2003.01924.x
Partial thyroxine-binding globulin (TBG) deficiency in a family with no detectable mutation of the TBG gene
Similar articles
-
A study on the inheritance of thyroxine-binding globulin (TBG) deficiency from data obtained in 13 families detected by a neonatal screening program.Clin Invest Med. 1988 Feb;11(1):34-9. Clin Invest Med. 1988. PMID: 3130208
-
Autosomally transmitted low concentration of thyroxine-binding globulin.Thyroid. 1999 Feb;9(2):159-63. doi: 10.1089/thy.1999.9.159. Thyroid. 1999. PMID: 10090316
-
A novel mutation causing complete thyroxine-binding globulin deficiency (TBG-CD-Negev) among the Bedouins in southern Israel.J Clin Endocrinol Metab. 2000 Oct;85(10):3687-9. doi: 10.1210/jcem.85.10.6899. J Clin Endocrinol Metab. 2000. PMID: 11061524 Clinical Trial.
-
[Inherited abnormality of thyroxine-binding globulin: its gene abnormality and pathogenesis].Nihon Rinsho. 1994 Apr;52(4):880-5. Nihon Rinsho. 1994. PMID: 8196174 Review. Japanese.
-
[Thyroxine-binding globulin gene and variants].Nihon Rinsho. 2006 May 28;Suppl 1:508-12. Nihon Rinsho. 2006. PMID: 16776202 Review. Japanese. No abstract available.
Cited by
-
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.J Clin Endocrinol Metab. 2015 Jan;100(1):E173-81. doi: 10.1210/jc.2014-3490. J Clin Endocrinol Metab. 2015. PMID: 25361180 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous