Associated Papers
Benign hereditary chorea: an update.
Inzelberg R et al.
Parkinsonism & Related Disorders, 2011
Genetics and phenomics of hypothyroidism and thyroid dys- and agenesis due to PAX8 and TTF1 mutations.
Montanelli L et al.
Molecular and Cellular Endocrinology, 2010
Choreoathetosis, hypothyroidism, and pulmonary alterations due to human NKX2-1 haploinsufficiency.
Krude H et al.
The Journal of Clinical Investigation, 2002
Select a paper to view details