A candidate gene for human neurodegenerative disorders: a rat PKCγ mutation causes a Parkinsonian syndrome
✍ Scribed by Craig, Nicola J.; Durán Alonso, María B.; Hawker, Kim L.; Shiels, Paul; Glencorse, Thora A.; Campbell, Jacqueline M.; Bennett, Neil K.; Canham, Maurice; Donald, Denise; Gardiner, Mary; Gilmore, Desmond P.; MacDonald, Raymond J.; Maitland, Kirsty; McCallion, Andrew S.; Russell, David; Payne, Anthony P.; Sutcliffe, Roger G.; Davies, R. Wayne
- Book ID
- 109941155
- Publisher
- Nature Publishing Group
- Year
- 2001
- Tongue
- English
- Weight
- 101 KB
- Volume
- 4
- Category
- Article
- ISSN
- 1097-6256
- DOI
- 10.1038/nn740
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## Communicated by A. Jamie Cuticchia There is a need for country/population-specific databases because the existence of population-specific mutations for single gene disorders is well documented, and there is also good evidence for ethnic differences in the frequencies of genetic variations invol