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

Crossref DOI link: https://doi.org/10.14310/horm.2002.1733

Published Online: 2017-07-30

Published Print: 2017-04

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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