Mutation inADORA1identified as likely cause of early-onset parkinsonism and cognitive dysfunction-Reference-Cited by-同舟云学术

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Mutation inADORA1identified as likely cause of early-onset parkinsonism and cognitive dysfunction

Published:2016-05-02 Issue:7 Volume:31 Page:1004-1011
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Jaberi Elham¹,Rohani Mohammad²,Shahidi Gholam Ali²,Nafissi Shahriar³,Arefian Ehsan¹,Soleimani Masoud⁴,Moghadam Abolfazl¹,Arzenani Mohsen Karimi⁵,Keramatian Farid⁶,Klotzle Brandy⁷,Fan Jian-Bing⁷,Turk Casey⁷,Steemers Frank⁷,Elahi Elahe¹⁶

Affiliation:

1. School of Biology, College of Science, University of Tehran; Tehran Iran

2. Department of Neurology; Hazrat Rasool Hospital, Iran University of Medical Sciences; Tehran Iran

3. Department of Neurology; Tehran University of Medical Sciences; Tehran Iran

4. School of Medical Sciences; Tarbiat Modares University; Tehran Iran

5. Center for Molecular Medicine; Karolinska Hospital; Stockholm Sweden

6. Department of Biotechnology; College of Science, University of Tehran; Tehran Iran

7. Illumina; San Diego California USA

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference56 articles.

1. Prevalence of Parkinson's disease in the elderly: the Rotterdam Study;Rijk;Neurology,1995

2. Understanding the molecular causes of Parkinson's disease;Wood-Kaczmar;Trends Mol Med,2006

3. Parkinson's disease: mechanisms and models;Dauer;Neuron,2003

4. A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients;Shojaee;Mov Disord,2009

5. Genome-wide linkage analysis of a Parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays;Shojaee;Am J Hum Genet,2008

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