Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia-Reference-Cited by-同舟云学术

Hyperthyroxinemia and Hypercortisolemia due to Familial Dysalbuminemia

Published:2020-11-01 Issue:11 Volume:30 Page:1681-1684
ISSN:1050-7256
Container-title:Thyroid
language:en
Short-container-title:Thyroid

Author:

Moran Carla¹,Seger Christoph²,Taylor Kevin³,Oddy Susan³,Burling Keith³,Rajanayagam Odelia¹,Fairall Louise⁴,McGowan Anne¹,Lyons Greta¹,Halsall David³,Gurnell Mark¹,Schwabe John⁴,Chatterjee Krishna¹,Strey Christopher⁵

Affiliation:

1. Wellcome Trust-MRC Institute of Metabolic Science, University of Cambridge, Cambridge, United Kingdom.

2. Risch Laboratory Group, Lagerstrasse, Buchs, SG, Switzerland.

3. Department of Clinical Biochemistry, Addenbrooke's Hospital, Cambridge, United Kingdom.

4. Institute of Structural and Chemical Biology, University of Leicester, Leicester, United Kingdom.

5. eSwiss Medical and Surgical Center, St. Gallen, Switzerland.

Publisher

Mary Ann Liebert Inc

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2020.0315

Reference4 articles.

1. Inherited defects of thyroxine-binding proteins

2. A Novel Missense Mutation in Codon 218 of the Albumin Gene in a Distinct Phenotype of Familial Dysalbuminemic Hyperthyroxinemia in a Japanese Kindred

3. Familial Dysalbuminemic Hyperthyroxinemia in a Swiss Family Caused by a Mutant Albumin (R218P) Shows an Apparent Discrepancy between Serum Concentration and Affinity for Thyroxine

4. Interaction of glucocorticoids and progesterone derivatives with human serum albumin

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