Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China. (Q54686961)

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scientific article published on 19 March 2010

Language	Label	Description	Also known as
English	Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China.	scientific article published on 19 March 2010

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Lack of association between ATP13A2 Ala746Thr variant and Parkinson's disease in Han population of mainland China. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Parkinson's disease

1 reference

based on heuristic

inferred from title

10

object named as

Sheng-Di Chen

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

author name string

Qing-Zhou Fei

1

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Li Cao

2

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Qin Xiao

3

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Ting Zhang

4

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Lan Zheng

5

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Xi-Jin Wang

6

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Gang Wang

7

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Hai-Yan Zhou

8

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Ying Wang

9

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

language of work or name

0 references

publication date

19 March 2010

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Neuroscience Letters

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

475

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

2

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

61-63

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

4 November 2023

https://opencitations.net/index/coci/api/v1/citations/10.1038/33416

Identifiers

10.1016/J.NEULET.2010.03.018

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 June 2018

http://europepmc.org/abstract/MED/20227461

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