Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study-Reference-Cited by-同舟云学术

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

Published:2008-07 Issue:7 Volume:7 Page:583-590
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Healy Daniel G,Falchi Mario,O'Sullivan Sean S,Bonifati Vincenzo,Durr Alexandra,Bressman Susan,Brice Alexis,Aasly Jan,Zabetian Cyrus P,Goldwurm Stefano,Ferreira Joaquim J,Tolosa Eduardo,Kay Denise M,Klein Christine,Williams David R,Marras Connie,Lang Anthony E,Wszolek Zbigniew K,Berciano Jose,Schapira Anthony HV,Lynch Timothy,Bhatia Kailash P,Gasser Thomas,Lees Andrew J,Wood Nicholas W

Publisher

Elsevier BV

Subject

Clinical Neurology

Reference33 articles.

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4. Clinical and pathologic features of families with LRRK2-associated Parkinson's disease;Whaley;J Neural Transm,2006

5. LRRK2 G2019S as a cause of Parkinson's disease in north African Arabs;Lesage;N Engl J Med,2006

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