# Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the<i>TITF1/NKX2-1</i>gene

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/benign-hereditary-chorea-phenotype-prognosis-therapeutic-outcome-and-long-term/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Domitille Gras,Laurence Jonard,Emmanuel Roze,Sandra Chantot‐Bastaraud,Jeanette Koht,Jacques Motté,Diana Rodriguez,Malek Louha,Isabelle Caubel,Isabelle Kemlin,Laurence Lion‐François,Cyril Goizet,Loïc Guillot,Marie‐Laure Moutard,Ralph Epaud,Bénédicte Héron,Perrine Charles,Marilyn Tallot,Agnès Camuzat,Alexandra Dürr,Michel Polak,David Devos,Damien Sanlaville,Isabelle Vuillaume,Thierry Billette de Villemeur,Marie Vidailhet,Diane Doummar |
| Citations | 127 |
| DOI | 10.1136/jnnp-2012-302505 |
| Fields | Biochemistry, Genetics and Molecular Biology,Medicine,Neuroscience |
| Open Access | false |
| OA Status | closed |
| OpenAlex ID | https://openalex.org/W2140915491 |
| PMID | 22832740 |
| Type | article |
| Year | 2012 |

## Paper authors

- [Jacques Motté](https://scholariq.org/researchers/jacques-motte/)

## Paper journal

- [Journal of Neurology Neurosurgery & Psychiatry](https://scholariq.org/journals/journal-of-neurology-neurosurgery-and-psychiatry/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Glycogen Storage Diseases and Myoclonus](https://scholariq.org/topics/glycogen-storage-diseases-and-myoclonus/)
- [Neurological diseases and metabolism](https://scholariq.org/topics/neurological-diseases-and-metabolism/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.