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Congenital central hypothyroidism (CCH) is a very rare disease. Alterations in pituitary development genes as well as mutations of immunoglobulin superfamily member 1 and transducin β-like protein 1 can result in CCH and multiple pituitary hormone d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3566::e9160759d9f69959fe1c99f9708a9d09
