| pubmed-article:21779299 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:21779299 | lifeskim:mentions | umls-concept:C0242422 | lld:lifeskim |
| pubmed-article:21779299 | lifeskim:mentions | umls-concept:C0026882 | lld:lifeskim |
| pubmed-article:21779299 | lifeskim:mentions | umls-concept:C0017768 | lld:lifeskim |
| pubmed-article:21779299 | lifeskim:mentions | umls-concept:C0332281 | lld:lifeskim |
| pubmed-article:21779299 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:21779299 | pubmed:dateCreated | 2011-7-22 | lld:pubmed |
| pubmed-article:21779299 | pubmed:abstractText | Gaucher's disease is an autosomal recessive, lysosomal storage disease caused by mutations of the ?-glucocerebrosidase gene (GBA). There is increasing evidence that GBA mutations are a genetic risk factor for the development of Parkinson's disease (PD). We report herein a family of Koreans exhibiting parkinsonism-associated GBA mutations. | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:commentsCorrections | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:language | eng | lld:pubmed |
| pubmed-article:21779299 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:21779299 | pubmed:status | PubMed-not-MEDLINE | lld:pubmed |
| pubmed-article:21779299 | pubmed:month | Jun | lld:pubmed |
| pubmed-article:21779299 | pubmed:issn | 2005-5013 | lld:pubmed |
| pubmed-article:21779299 | pubmed:author | pubmed-author:LeeSarahS | lld:pubmed |
| pubmed-article:21779299 | pubmed:author | pubmed-author:LeePhil HyuPH | lld:pubmed |
| pubmed-article:21779299 | pubmed:author | pubmed-author:KimSeung-MinS... | lld:pubmed |
| pubmed-article:21779299 | pubmed:author | pubmed-author:SunwooMun-Kyu... | lld:pubmed |
| pubmed-article:21779299 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:21779299 | pubmed:volume | 7 | lld:pubmed |
| pubmed-article:21779299 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:21779299 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:21779299 | pubmed:pagination | 99-101 | lld:pubmed |
| pubmed-article:21779299 | pubmed:year | 2011 | lld:pubmed |
| pubmed-article:21779299 | pubmed:articleTitle | Parkinsonism associated with glucocerebrosidase mutation. | lld:pubmed |
| pubmed-article:21779299 | pubmed:affiliation | Department of Neurology, Yonsei University College of Medicine, Seoul, Korea. | lld:pubmed |
| pubmed-article:21779299 | pubmed:publicationType | Journal Article | lld:pubmed |
