Associated Papers
Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism.
Bruellman RJ et al.
The Journal of Clinical Endocrinology and Metabolism, 2020
Benign Hereditary Chorea: An Update.
Peall KJ et al.
Tremor and Other Hyperkinetic Movements (new York, N.y.), 2015
Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literature.
Nettore IC et al.
Thyroid : Official Journal of the American Thyroid Association, 2013
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