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 (Q42510161)
Jump to navigation
Jump to search
scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
scientific article |
Statements
1 reference
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 (English)
1 reference
1 reference
Thierry Billette de Villemeur
1 reference
Marie Vidailhet
1 reference
Alexandra Durr
1 reference
Emmanuel Roze
1 reference
Perrine Charles
1 reference
Sandra Chantot-Bastaraud
1 reference
Domitille Gras
1 reference
Laurence Jonard
1 reference
Jacques Motte
1 reference
Diana Rodriguez
1 reference
Malek Louha
1 reference
Isabelle Caubel
1 reference
Isabelle Kemlin
1 reference
Laurence Lion-François
1 reference
Cyril Goizet
1 reference
Marie-Laure Moutard
1 reference
Ralph Epaud
1 reference
Bénédicte Héron
1 reference
Marilyn Tallot
1 reference
Agnès Camuzat
1 reference
Michel Polak
1 reference
Isabelle Vuillaume
1 reference
Diane Doummar
1 reference
24 July 2012
1 reference
1 reference
83
1 reference
10
1 reference
956-962
1 reference
Identifiers
1 reference
1 reference