Cite
HARVARD Citation
Novara, F. et al. (2017). Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan–Herndon–Dudley Syndrome. Human mutation. 38 (3), pp. 260-264. [Online].
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Novara, F. et al. (2017). Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan–Herndon–Dudley Syndrome. Human mutation. 38 (3), pp. 260-264. [Online].