Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea

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Title
Functional characterization of two novel mutations in TTF-1/NKX2.1 homeodomain in patients with benign hereditary chorea
Authors
Keywords
Benign hereditary chorea, TTF-1/Nkx2.1, Brain–thyroid–lung syndrome, Genotype/phenotype correlation, Neurological disease
Journal
JOURNAL OF THE NEUROLOGICAL SCIENCES
Volume 360, Issue -, Pages 78-83
Publisher
Elsevier BV
Online
2015-11-27
DOI
10.1016/j.jns.2015.11.050

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