期刊
HUMAN MOLECULAR GENETICS
卷 18, 期 2, 页码 341-346出版社
OXFORD UNIV PRESS
DOI: 10.1093/hmg/ddn340
关键词
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资金
- National Institute on Aging
- National Institutes of Health
- Department of Health and Human Services [Z01-AG000957-05]
- Fundacao para a Ciencia e Tecnologia [SFRH/BD/29647/2006]
- Fundação para a Ciência e a Tecnologia [SFRH/BD/29647/2006] Funding Source: FCT
Mutations in GIGYF2 have recently been described as causative of Parkinson's disease in Europeans. In an attempt to replicate these results in independent populations, we sequenced the entire coding region of GIGYF2 in a large series of Portuguese and North American samples. We report the finding of two of the previously published mutations in neurologically normal Control individuals. This suggests that mutations in GIGYF2 are not strongly related to the development of the disease in either of these populations.
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