SCOPUS 정보 검색 플랫폼

Volumn 134, Issue 1, 1996, Pages 114-

Thyrotropin receptor mutations in hyperfunctioning thyroid adenomas: New mutants, new second messenger and new frequency

Author keywords

[No Author keywords available]

Indexed keywords

THYROTROPIN RECEPTOR;

HUMAN; MUTATION; NOTE; PRIORITY JOURNAL; THYROID ADENOMA;

EID: 13344269676 PISSN: 08044643 EISSN: None Source Type: Journal
DOI: 10.1530/eje.0.1340114 Document Type: Note

Times cited : (2)

References (3)

1
- 0029044073
- 2- cascades
- 2- cascades. Mol Endocrinol 1995;9:725-33
- (1995) Mol Endocrinol , vol.9 , pp. 725-733
- Parma, J.¹ Van Sande, J.² Swillens, S.³ Tonacchera, M.⁴ Dumont, J.⁵ Vassart, G.⁶

2
- 0028240982
- Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism
- Duprez L, Parma J, Van Sande J, et al. Germline mutations in the thyrotropin receptor gene cause non-autoimmune autosomal dominant hyperthyroidism. Nat Genet 1994;7:396-400
- (1994) Nat Genet , vol.7 , pp. 396-400
- Duprez, L.¹ Parma, J.² Van Sande, J.³

3
- 0028891649
- Brief report: Congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene
- Kopp P, Van Sande J, Parma J, et al. Brief report: congenital hyperthyroidism caused by a mutation in the thyrotropin-receptor gene. N Engl J Med 1995;332:150-4
- (1995) N Engl J Med , vol.332 , pp. 150-154
- Kopp, P.¹ Van Sande, J.² Parma, J.³

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.