Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact-Reference-Cited by-同舟云学术

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Autosomal dominant Parkinson's disease caused by the recently identified LRRK2 N1437D mutation in a Chinese family: Clinical features, imaging findings, and functional impact

Published:2023-06 Issue: Volume:111 Page:105441
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Sun Yi-Min,Gan Lin-Hua,Peng Fang,Zhou Xin-Yue,Chen Qi-Si,Liu Feng-Tao,Tang Yi-Lin,Wu Ping,Lu Jia-Ying^ORCID,Ge Jing-Jie,Yen Tzu-Chen^ORCID,Zuo Chuan-Tao,Song Bin^ORCID,Wu Jian-Jun,Wang Jian^ORCID

Publisher

Elsevier BV

Subject

Neurology (clinical),Geriatrics and Gerontology,Neurology

Reference40 articles.

1. Parkinson's disease;Kalia;Lancet,2015

2. The genetic architecture of Parkinson's disease, the Lancet;Blauwendraat;Neurology,2020

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

4. LRRK2 kinase in Parkinson's disease;Alessi;Science,2018

5. Advances in the genetics of Parkinson's disease: a guide for the clinician;Sheerin;Movement disorders clinical practice,2014

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