| scholarly article | Q13442814 |
| P356 | DOI | 10.1002/ANA.10637 |
| P698 | PubMed publication ID | 12891678 |
| P50 | author | Peter Henry St George-Hyslop | Q7177066 |
| Ekaterina Rogaeva | Q30089881 | ||
| Anthony Lang | Q47504039 | ||
| Toshitaka Kawarai | Q58924545 | ||
| Sylvain Houle | Q61825758 | ||
| Galit Kleiner-Fisman | Q66811896 | ||
| Christine Sato | Q114422875 | ||
| P2093 | author name string | William Halliday | |
| Helena Medeiros | |||
| P433 | issue | 2 | |
| P921 | main subject | Huntington's disease | Q190564 |
| Benign hereditary chorea | Q24977061 | ||
| P304 | page(s) | 244-247 | |
| P577 | publication date | 2003-08-01 | |
| P1433 | published in | Annals of Neurology | Q564414 |
| P1476 | title | Benign hereditary chorea: clinical, genetic, and pathological findings | |
| P478 | volume | 54 |
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| Q37589830 | Comprehensive genotyping and clinical characterisation reveal 27 novel NKX2-1 mutations and expand the phenotypic spectrum |
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