LRRK2 haplotype-sharing analysis in Parkinson's disease reveals a novel p.S1761R mutation

Author:

Lorenzo-Betancor Oswaldo,Samaranch Lluís,Ezquerra Mario,Tolosa Eduardo,Lorenzo Elena,Irigoyen Jaione,Gaig Carles,Pastor María A.,Soto-Ortolaza Alexandra I.,Ross Owen A.,Rodríguez-Oroz María C.,Valldeoriola Francesc,Martí María J.,Luquin María R.,Perez-Tur Jordi,Burguera Juan A.,Obeso José A.,Pastor Pau

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference30 articles.

1. Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group;de Rijk;Neurology,2000

2. A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism;Munoz;Neurosci Lett,2000

3. Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism;Munoz;J Neurol Neurosurg Psychiatry,2002

4. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease;Di Fonzo;Lancet,2005

5. A common LRRK2 mutation in idiopathic Parkinson's disease;Gilks;Lancet,2005

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