Cite
HARVARD Citation
Fourneaux, R. et al. (2022). IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology. 187 (6), pp. 787-795. [Online].
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Fourneaux, R. et al. (2022). IGSF1 mutations are the most frequent genetic aetiology of thyrotropin deficiency. European journal of endocrinology. 187 (6), pp. 787-795. [Online].