(Q47349423)

English

Rapid screening of ATP13A2 variant with high-resolution melting analysis

scientific article published in October 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

Rapid screening of ATP13A2 variant with high-resolution melting analysis (English)

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

Manabu Funayama

1

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

3

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

Nobutaka Hattori

7

object named as

Nobutaka Hattori

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

Yoshikuni Mizuno

6

object named as

Yoshikuni Mizuno

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

Hiroyuki Tomiyama

2

object named as

Hiroyuki Tomiyama

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

4

object named as

Kotaro Ogaki

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

5

object named as

Hiroyo Yoshino

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

language of work or name

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publication date

1 October 2010

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

25

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

14

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

2434-2437

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

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

10.1002/MDS.23106

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

14 January 2018

http://europepmc.org/abstract/MED/20976737

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