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Is Benign Hereditary Chorea Really Benign? Brain‐Lung‐Thyroid Syndrome Caused by NKX2‐1 Mutations
BACKGROUND: Since its localization to the NKX2‐1 gene in 2002, the phenotype of the disorder historically called “benign hereditary chorea” has been expanding beyond chorea. METHODS: The phenomenology of movement disorders and other symptomatology associated with mutations in NKX2‐1 were characteriz...
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| Publicado no: | Mov Disord Clin Pract |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6335533/ https://ncbi.nlm.nih.gov/pubmed/30746413 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mdc3.12690 |
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