IGSF1 mutation as a cause of isolated central hypothyroidism
Endocrinol Diabetes Nutr (Engl Ed)
.
2022 Dec;69(10):913-914.
doi: 10.1016/j.endien.2022.11.032.
Epub 2022 Dec 1.
Authors
Julia Costas Eimil
1
,
Paula Sánchez-Sobrino
2
Affiliations
1
Servicio de Endocrinología y Nutrición, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain. Electronic address: julia.costas.eimil@sergas.es.
2
Servicio de Endocrinología y Nutrición, Complejo Hospitalario Universitario de Pontevedra, Pontevedra, Spain.
PMID:
36464600
DOI:
10.1016/j.endien.2022.11.032
No abstract available
Publication types
Letter
MeSH terms
Congenital Hypothyroidism*
Humans
Immunoglobulins / genetics
Membrane Proteins / genetics
Mutation
Substances
IGSF1 protein, human
Immunoglobulins
Membrane Proteins