The ancestry of LRRK2 Gly2019Ser parkinsonism - Authors' reply

The Lancet Neurology

Volumn 7, Issue 9, 2008, Pages 770-771

  Farrer, Matthew J ^a   Gibson, Rachel ^a   Hentati, Fayçal ^a  

^a MAYO CLINIC   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LEUCINE RICH REPEAT KINASE 2;

AFRICA; GENE MUTATION; GENETIC SIMILARITY; HEALTH CARE; LETTER; PARKINSONISM; PRIORITY JOURNAL; TUNISIA;

EID: 48849117757     PISSN: 14744422     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1474-4422(08)70179-0     Document Type: Letter

References (4)

1. Brett M., and Fentress E. The Berbers (1997), Blackwell, Oxford
2. Maddy-Weitzman B. Ethno-politics and globalization in north Africa: the Berber culture movement. J N Af Stud 11 (2006) 71-84
3. Farrer M.J. Genetics of Parkinson disease: paradigm shifts and future prospects. Nat Rev Genet 7 (2006) 306-318
4. Warren L., Gibson R., Ishihara L., et al. A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease. Parkinsonism Relat Disord 14 (2008) 77-80