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.

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

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