Analysis of the α-synuclein G209A mutation in familial Parkinson's disease [7]

Lancet

Volumn 351, Issue 9095, 1998, Pages 37-38

  Zareparsi, Sepideh ^a   Kay, Jeffrey ^b   Camicioli, Richard ^b   Kramer, Patricia ^b   Nutt, John ^b   Bird, Thomas ^b   Litt, Michael ^b   Payami, Haydeh ^b  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; AUTOPSY; CHROMOSOME 4Q; FAMILIAL DISEASE; GENE MUTATION; GENETIC LINKAGE; GREECE; HUMAN; LETTER; LEWY BODY; MAJOR CLINICAL STUDY; ONSET AGE; PARKINSON DISEASE; PRIORITY JOURNAL; SUBSTANTIA NIGRA;

EID: 0032477559     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(05)78089-2     Document Type: Article

References (5)

1. 1 Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation in the a-synuclein gene identified in families with Parkinson's disease. Science 1997; 276: 2045-47.
2. 2 Hughes AJ, Daniel SE, Kilford L, Lees AJ. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. J Neurol Neurosurg Psychiatry 1992; 55: 181-84.
3. 3 Polymeropoulos MH, Higgins JJ, Golbe LI, et al. Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science 1996; 274: 1197-99.
4. 4 Scott WK, Stajich JM, Yamaoka LH, et al. Genetic complexity and Parkinson's disease. Science 1997; 277: 387-88.
5. 5 Gasser T, Muller-Myhsok B, Wszolek ZK, et al. Genetic complexity and Parkinson's disease. Science 1997; 277: 388-89.