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SAT-546 Discovering the Function of IGSF1 and Its Role in the Hypothalamic-Pituitary-Thyroid Axis
Loss of function mutations in the X-linked immunoglobulin superfamily, member 1 (IGSF1) gene cause congenital central hypothyroidism, hypoprolactinemia, macroorchidism, and the dysregulation of growth hormone and pubertal development. IGSF1 is a type 1 transmembrane protein of unknown function that...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552037/ http://dx.doi.org/10.1210/js.2019-SAT-546 |