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Frontiers in Endocrinology, ISSN 1664-2392, 08/2017, Volume 8, p. 198
Journal Article
Thyroid Research, ISSN 1756-6614, 2011, Volume 4, Issue 1, pp. I1 - I1
Journal Article
Journal Article
PLoS Genetics, ISSN 1553-7390, 04/2010, Volume 6, Issue 4, p. e1000916
Journal Article
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, ISSN 1422-0067, 11/2019, Volume 20, Issue 22, p. 5564
(1) Background: Central congenital hypothyroidism (CCH) is a rare endocrine disorder that can be caused by mutations in the beta-subunit of thyrotropin (TSHB).... 
GENE-MUTATIONS | CONGENITAL CENTRAL HYPOTHYROIDISM | G-protein coupled receptors | HOMOZYGOUS MUTATION | BIOCHEMISTRY & MOLECULAR BIOLOGY | HUMAN CHORIONIC-GONADOTROPIN | SITE-DIRECTED MUTAGENESIS | CHEMISTRY, MULTIDISCIPLINARY | TSHR | DEFICIENCY | REGION | thyroid-stimulating hormone | HYPOPITUITARISM | central congenital hypothyroidism | HUMAN THYROTROPIN RECEPTOR | GTP-Binding Protein alpha Subunits, Gq-G11 - genetics | Thyrotropin, beta Subunit - genetics | Receptors, Thyrotropin - genetics | Receptors, Thyrotropin - metabolism | Humans | Congenital Hypothyroidism - metabolism | Thyrotropin, beta Subunit - chemistry | Extracellular Signal-Regulated MAP Kinases - metabolism | Extracellular Signal-Regulated MAP Kinases - genetics | MAP Kinase Signaling System | Thyrotropin, beta Subunit - metabolism | Congenital Hypothyroidism - genetics | HEK293 Cells | Cell Line, Tumor | Protein Domains | Cyclic AMP - genetics | Mutation | Receptors, Thyrotropin - chemistry | GTP-Binding Protein alpha Subunits, Gq-G11 - metabolism | Cyclic AMP - metabolism | Second Messenger Systems | Congenital diseases | Deactivation | Peptides | Fluorescence | Amino acids | MAP kinase | Glycoproteins | Hypothyroidism | Patients | Mutants | Proteins | Luminous intensity | Signaling | Genotype & phenotype | g-protein coupled receptors | tshr
Journal Article
The Lancet, ISSN 0140-6736, 10/2004, Volume 364, Issue 9443, pp. 1435 - 1437
Journal Article