Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene
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| Description | scientific article |
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author: David Devos Marie Vidailhet Alexandra Durr Thierry Billette de Villemeur Perrine Charles Emmanuel Roze Jeanette Koht Sandra Chantot-Bastaraud Damien Sanlaville Loic Guillot |
| Publication date | July 24, 2012 |
| Language | English |
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