Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations-Reference-Cited by-同舟云学术

Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

Published:2005-04 Issue:4 Volume:76 Page:672-680
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Kachergus Jennifer,Mata Ignacio F.,Hulihan Mary,Taylor Julie P.,Lincoln Sarah,Aasly Jan,Gibson J. Mark,Ross Owen A.,Lynch Timothy,Wiley Joseph,Payami Haydeh,Nutt John,Maraganore Demetrius M.,Czyzewski Krzysztof,Styczynska Maria,Wszolek Zbigniew K.,Farrer Matthew J.,Toft Mathias

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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