Associated Papers
Identification of a Novel Nonsense Mutation in the IGSF1 Gene Reveals Sex-Specific Phenotypic Variability Within a Single Family.
Ruta R et al.
Children (basel, Switzerland), 2025
Diagnosis and Management of Central Congenital Hypothyroidism.
Lauffer P et al.
Frontiers in Endocrinology, 2021
34566885 (PubMed )
Supplement: Table_1.docx
From Consternation to Revelation: Discovery of a Role for IGSF1 in Pituitary Control of Thyroid Function.
Bernard DJ et al.
Journal of the Endocrine Society, 2018
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