PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability-Reference-Cited by-同舟云学术

PTRHD1 Loss-of-function mutation in an african family with juvenile-onset Parkinsonism and intellectual disability

Published:2018-11 Issue:11 Volume:33 Page:1814-1819
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Kuipers Demy J.S.¹,Carr Jonathan²,Bardien Soraya³,Thomas Pearl²,Sebate Boiketlo³,Breedveld Guido J.¹,van Minkelen Rick¹,Brouwer Rutger W.W.⁴,van Ijcken Wilfred F.J.⁴,van Slegtenhorst Marjon A.¹,Bonifati Vincenzo¹,Quadri Marialuisa¹

Affiliation:

1. Department of Clinical Genetics; Erasmus MC; Rotterdam The Netherlands

2. Division of Neurology, Faculty of Medicine and Health Sciences; Stellenbosch University; Cape Town South Africa

3. Division of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences; Stellenbosch University; Cape Town South Africa

4. Center for Biomics, Erasmus Medical Center; Rotterdam The Netherlands

Funder

National Research Foundation of South Africa to J.C.

South African Medical Research Council

National Research Foundation of South Africa

Stichting ParkinsonFonds

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.27501/fullpdf

Reference16 articles.

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4. The prevalence of Parkinson's disease in rural Tanzania;Dotchin;Mov Disord,2008

5. Projection of the prevalence of Parkinson's disease in the coming decades: revisited;Rossi;Mov Disord,2018

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