Genetic disorders of thyroid development, hormone biosynthesis and signalling
Author:
Affiliation:
1. Wellcome Trust‐MRC Institute of Metabolic Science University of Cambridge Cambridge UK
2. Department of Internal Medicine Erasmus Medical Center, Academic Center for Thyroid Diseases Rotterdam The Netherlands
Funder
Erasmus Medisch Centrum
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14817
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3. A New PAX8 Mutation Causing Congenital Hypothyroidism in Three Generations of a Family Is Associated with Abnormalities in the Urogenital Tract
4. A NovelFOXE1Mutation (R73S) in Bamforth–Lazarus Syndrome Causing Increased Thyroidal Gene Expression
5. The role of GLIS3 in thyroid disease as part of a multisystem disorder
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