Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration-Reference-Cited by-同舟云学术

Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration

Published:2008-07 Issue:1-2 Volume:270 Page:94-98
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Gaig Carles,Ezquerra Mario,Martí Maria José,Valldeoriola Francesc,Muñoz Esteban,Lladó Albert,Rey Maria Jesús,Cardozo Adriana,Molinuevo José Luis,Tolosa Eduardo

Publisher

Elsevier BV

Subject

Neurology (clinical),Neurology

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4. LRRK2 mutations in Spanish patients with Parkinson's disease: frequency, clinical features and incomplete penetrance;Gaig;Arch Neurol,2006

5. LRRK2 and Lewy body disease;Ross;Ann Neurol,2006

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