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Novel SLC16A2 mutations in patients with Allan-Herndon-Dudley syndrome

Keiko Shimojima1, Koichi Maruyama2, Masahiro Kikuchi3

  • 1Tokyo Women's Medical University Institute for Integrated Medical Sciences, Tokyo, Japan.

Intractable & Rare Diseases Research
|September 28, 2016
PubMed

Keywords:
Thyroid functiondelayed myelinationmonocarboxylate transporter 8 (MCT8)

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