Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene

  1. Rego, T.
  2. Lado, C.G.
  3. Rodríguez, P.C.
  4. Santos, F.S.
  5. Angueira, F.B.
  6. Castro-Feijóo, L.
  7. Conde, J.B.
  8. Castro-Gago, M.
Journal:
Hormones

ISSN: 2520-8721,  1109-3099

Year of publication: 2017

Volume: 16

Issue: 2

Pages: 194-199

Type: Article

DOI: 10.14310/HORM.2002.1733 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus