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Novel IGSF1 mutation in two brothers with congenital central hypothyroidism. A form of hypothyroidism that escapes neonatal screening

Crossref DOI link: https://doi.org/10.1016/j.anpede.2026.504177

Published Print: 2026-05

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

García-García, Emilio

Rodríguez-Rodríguez, Ana

Macher, Hada C.

García de Veas, José Luis
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Text and Data Mining valid from 2026-05-01

Text and Data Mining valid from 2026-05-01

Version of Record valid from 2026-04-14
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This article is maintained by: Elsevier

Article Title: Novel IGSF1 mutation in two brothers with congenital central hypothyroidism. A form of hypothyroidism that escapes neonatal screening

Journal Title: Anales de Pediatría (English Edition)

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.anpede.2026.504177

CrossRef DOI link to the associated document: https://doi.org/10.1016/j.anpedi.2026.504177

Content Type: article

Copyright: © 2026 Asociación Española de Pediatría. Published by Elsevier España, S.L.U.