| pubmed-article:16476943 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:16476943 | lifeskim:mentions | umls-concept:C0032659 | lld:lifeskim |
| pubmed-article:16476943 | lifeskim:mentions | umls-concept:C0030567 | lld:lifeskim |
| pubmed-article:16476943 | lifeskim:mentions | umls-concept:C0337812 | lld:lifeskim |
| pubmed-article:16476943 | lifeskim:mentions | umls-concept:C0017768 | lld:lifeskim |
| pubmed-article:16476943 | lifeskim:mentions | umls-concept:C0596611 | lld:lifeskim |
| pubmed-article:16476943 | pubmed:issue | 3 | lld:pubmed |
| pubmed-article:16476943 | pubmed:dateCreated | 2006-2-14 | lld:pubmed |
| pubmed-article:16476943 | pubmed:abstractText | An association between mutations in the glucocerebrosidase (GBA) gene and Parkinson disease (PD) was recently reported in Ashkenazi Jews. The authors screened a series of 311 Norwegian patients with PD and 474 controls for 2 common functional mutations of the GBA protein, N370S and L444P. Seven patients (2.3%) and 8 controls (1.7%) carried a mutant GBA allele (p = 0.58). This study does not indicate increased susceptibility to PD in GBA mutations carriers in Norway. | lld:pubmed |
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| pubmed-article:16476943 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:16476943 | pubmed:citationSubset | AIM | lld:pubmed |
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| pubmed-article:16476943 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:16476943 | pubmed:month | Feb | lld:pubmed |
| pubmed-article:16476943 | pubmed:issn | 1526-632X | lld:pubmed |
| pubmed-article:16476943 | pubmed:author | pubmed-author:RossO AOA | lld:pubmed |
| pubmed-article:16476943 | pubmed:author | pubmed-author:TobéFF | lld:pubmed |
| pubmed-article:16476943 | pubmed:author | pubmed-author:FarrerM JMJ | lld:pubmed |
| pubmed-article:16476943 | pubmed:author | pubmed-author:AaslyJ OJO | lld:pubmed |
| pubmed-article:16476943 | pubmed:author | pubmed-author:PielstickerLL | lld:pubmed |
| pubmed-article:16476943 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:16476943 | pubmed:day | 14 | lld:pubmed |
| pubmed-article:16476943 | pubmed:volume | 66 | lld:pubmed |
| pubmed-article:16476943 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:16476943 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:16476943 | pubmed:pagination | 415-7 | lld:pubmed |
| pubmed-article:16476943 | pubmed:dateRevised | 2007-11-14 | lld:pubmed |
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| pubmed-article:16476943 | pubmed:year | 2006 | lld:pubmed |
| pubmed-article:16476943 | pubmed:articleTitle | Glucocerebrosidase gene mutations and Parkinson disease in the Norwegian population. | lld:pubmed |
| pubmed-article:16476943 | pubmed:affiliation | Department of Neuroscience, Norwegian University of Science and Technology, N-7489 Trondheim, Norway. mathias.toft@ntnu.no | lld:pubmed |
| pubmed-article:16476943 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:16476943 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:16476943 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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