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A novel germline mutation in the thyrotropin receptor (TSHR) gene causing nonautoimmune congenital hyperthyroidism
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Kohler, B.1
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46
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Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene
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47
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0029973239
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48
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1842353339
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Congenital nonautoimmune hyperthyroidism caused by a new sporadic germline mutation in the thyrotropin receptor gene
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Abstract
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Holzapfel H.P., Wonerow P., Henshen M., Petrykowski W., Scherbaum W.A., Paschke R. Congenital nonautoimmune hyperthyroidism caused by a new sporadic germline mutation in the thyrotropin receptor gene. J. Endocrinol. Invest. 19 (Suppl. 6): 25, 1996. (Abstract).
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49
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Abstract
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Esapa C.T., Betts P., Kendall-Taylor P., Harris P.E. A novel TSH receptor mutation in an infant with thyrotoxicosis. J. Endocrinol. Invest. 19 (Suppl. 6): 71, 1996. (Abstract).
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50
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Constitutive activation of the Gs-α protein-adenylate cyclase pathway may not be sufficient to generate toxic thyroid adenomas
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51
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52
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Asteria C., Persani L., Romoli R., Beck-Peccoz P. Resistance to thyrotropin action resulting from inactivating mutation of thyrotropin receptor (TSH-R) gene. J. Endocrinol. Invest. 19 (Suppl. 6). 26, 1996. (Abstract).
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Sporadic congenital hypothyroidism due to compound heterozygosity for two mutations of the coding sequence of the thyrotropin receptor gene
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Biebermann H., Krude H., Thiede C., Kotulla P., Gruters A. Sporadic congenital hypothyroidism due to compound heterozygosity for two mutations of the coding sequence of the thyrotropin receptor gene. 10th International Congress of Endocrinology, San Francisco, USA. P2-954, 1996 (Abstract).
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54
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