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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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| Gepubliceerd in: | Pediatr Neurol Briefs |
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| Hoofdauteur: | |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Pediatric Neurology Briefs Publishers
2015
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| Onderwerpen: | |
| Online toegang: | 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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