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ADCY5 Mutations and Benign Hereditary Chorea
Investigators from the Institute of Neurology, London, UK, and centers in Italy, Germany, and Greece, studied 18 unrelated cases of benign hereditary chorea BHC (7 familial, 11 sporadic) who were negative for NKX2-1 mutations.
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| Vydáno v: | Pediatr Neurol Briefs |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Pediatric Neurology Briefs Publishers
2015
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4747282/ https://ncbi.nlm.nih.gov/pubmed/26933606 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15844/pedneurbriefs-29-9-5 |
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