Rapid detection of a point mutation in thyroid-stimulating hormoneβ-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency
Open Access
- 1 December 1991
- journal article
- case report
- Published by Springer Nature in Journal of Human Genetics
- Vol. 36 (4) , 313-316
- https://doi.org/10.1007/bf01883604
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Deletion Pattern in the 21-Hydroxylase Gene Detected by Polymerase Chain ReactionPediatrics International, 1991
- Deoxyribonucleic Acid Analyses of Five Families with Familial Inherited Thyroid Stimulating Hormone Deficiency*Journal of Clinical Endocrinology & Metabolism, 1990
- Molecular cloning of the human thyrotropin-β subunit geneFEBS Letters, 1985
- Familial Isolated Thyrotropin Deficiency with CretinismNew England Journal of Medicine, 1971