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Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset
OBJECTIVE: To characterize sequence variation within the glucocerebrosidase (GBA) gene in a select subset of our sample of patients with familial Parkinson disease (PD) and then to test in our full sample whether these sequence variants increased the risk for PD and were associated with an earlier o...
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| Hlavní autoři: | , , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
American Academy of Neurology
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2677501/ https://ncbi.nlm.nih.gov/pubmed/18987351 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/01.wnl.0000327823.81237.d1 |
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