Movement disorders in MCT8 deficiency/Allan-Herndon-Dudley Syndrome.
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Masnada S, et al. Among authors: fadilah a.
Mol Genet Metab. 2022 Jan;135(1):109-113. doi: 10.1016/j.ymgme.2021.12.003. Epub 2021 Dec 16.
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PMID: 34969638