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IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency

Document Type

Article

Author

Fourneaux, R.; Reynaud, R.; Mougel, G.; Castets, S.; Barlier, A.; Brue, T.; Castinetti, F.; Saveanu, A.; Bretones, P.; Dauriat, B.; Edouard, T.; Raverot, G.

Source

In: European Journal of Endocrinology. (European Journal of Endocrinology, December 2022, 187(6):787-795)

Subject

Language

English

ISSN

1479683X
08044643

Online Access

Full Text (Oxford University Press) Web of Science JCR 저널정보 Scopus Find it@PNU

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