Found: 4
Select item for more details and to access through your institution.
Atypical juvenile parkinsonism in a consanguineous SPG15 family.
- Published in:
- Movement Disorders, 2011, v. 26, n. 3, p. 565, doi. 10.1002/mds.23472
- By:
- Publication type:
- Article
Common variants at VRK2 and TCF4 conferring risk of schizophrenia.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 20, p. 4076, doi. 10.1093/hmg/ddr325
- By:
- Publication type:
- Article
A mutation in APP protects against Alzheimer's disease and age-related cognitive decline.
- Published in:
- Nature, 2012, v. 488, n. 7409, p. 96, doi. 10.1038/nature11283
- By:
- Publication type:
- Article
Heterozygote carriers for CNVs in PARK2 are at increased risk of Parkinson's disease.
- Published in:
- Human Molecular Genetics, 2015, v. 24, n. 19, p. 5637, doi. 10.1093/hmg/ddv277
- By:
- Publication type:
- Article