Citations for
1SERPINA7
A novel mutation (del 1711 G) in the TBG gene as a cause of complete TBG deficiency.
Lacka K, Nizankowska T, Ogrodowicz A, Lacki JK.
Thyroid 17(11):1143-6. 2007
2SERPINA7, TBG
TBG deficiency: description of two novel mutations associated with complete TBG deficiency and review of the literature.
Mannavola D, Vannucchi G, Fugazzola L, Cirello V, Campi I, Radetti G, Persani L, Refetoff S, Beck-Peccoz P.
J Mol Med 84(10):864-71. Epub 2006 Sep 1. Review. 2006
3SERPINA7, TBG
Precise localization of the human thyroxine-binding globulin gene to chromosome Xq22.2 by fluorescence in situ hybridization.
Mori Y, et al.
Hum Genet 96 : 481-482. 1995
4SERPINA7, TBG
Gene screening in Japanese families with complete deficiency of thyroxine-binding globulin demonstrates that a nucleotide deletion at codon 352 may be a race specific mutation.
Takeda K, et al.
Clin Endocrinol 40 : 221-226. 1994
5SERPINA7, TBG
The structure of the human thyroxine binding globulin (TBG) gene.
Akbari MT, et al.
Biochim Biophys Acta 1216 : 446-454. 1993
6SERPINA7, TBG
Molecular basis of inherited thyroxine-binding globulin defects.
Janssen OE, et al.
Trends Endocrinol Metab 3 : 49-53. 1992
7SERPINA7, TBG
Thyroxine-binding globulin variant (TBG-Kumamoto). Identification of a point mutation and genotype analysis of its family.
Shirotani T, et al.
Endocrinol Jpn 39 : 577-584. 1992
8SERPINA7, TBG
Sequence of the variant thyroxine-binding globulin (TBG) in a Montreal family with partial TBG deficiency.
Janssen OE, et al.
Hum Genet 87 : 119-122. 1991
9SERPINA7, TBG
Nucleotide deletion resulting in frameshift as a possible cause of complete thyroxine-binding globulin deficiency in six Japanese families.
Yamamori I, et al.
J Clin Endocrinol Metab 73 : 262-267. 1991
10SERPINA7, TBG
Sequencing of the variant thyroxine-binding globulin (TBG)-Quebec reveals two nucleotide substitutions.
Bertenshaw R, et al.
Am J Hum Genet 48 : 741-744. 1991
11SERPINA7, TBG
Localization of the human thyroxine-binding globulin gene to the long arm of the X chromosome (Xq21-22).
Trent JM, et al.
Am J Hum Genet 41 : 428-435. 1987
12SERPINA7, TBG
Complete amino acid sequence of human thyroxine-binding globulin deduced from cloned DNA : close homology to the serine antiproteases.
Flink IL, et al.
Proc Natl Acad Sci U S A 83 : 7708-7712. 1986
13SERPINA7, TBG
Detection of genetic variation with radioactive ligands. IV. X-linked polymorphic genetic variation of thyroxin-binding globulin (TGB).
Daiger SP, et al.
Am J Hum Genet 33 : 640-648. 1981
14SERPINA7, TBG
Hereditary abnormalities of thyroxine-binding globulin concentration : a study of 19 kindreds with inherited increase or decrease of thyroxine-binding globuline.
Burr WA, et al.
Q J Med 49 : 295-313. 1980