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Fourneaux, R., Reynaud, R., Mougel, G., Castets, S., Bretones, P., Dauriat, B., Edouard, T., Raverot, G., Barlier, A., Brue, T., Castinetti, F., & Saveanu, A. (2022). iGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology, 187(6), 787–795. http://access.bl.uk/ark:/81055/vdc_100177208887.0x00004e