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A novel
TITF-1
mutation causes benign hereditary chorea with response to levodopa
Neurology Asmus et al. 64: 1952
Data Supplement
Two tables; two Word documents.
Files in this Data Supplement:
E1
- Table 1. Genetic findings in pedigrees and patients with TITF-1 (Nkx2.1) mutations; Word document.
E2
- Table 2. Phenotypic findings in pedigrees and patients with TITF-1 (Nkx2.1) mutations; Word document.
This Article
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