(Q48471225)

English

C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation.

scientific article published in June 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. (English)

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

neurodegeneration with brain iron accumulation

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neurodegeneration

1 reference

based on heuristic

inferred from title

Luisa Chiapparini

7

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Barbara Garavaglia

10

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

12

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Valeria Tiranti

14

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

object named as

Chiara Reale

5

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object named as

Dario Brunetti

6

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object named as

Sabrina Dusi

4

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Celeste Panteghini

object named as

Celeste Panteghini

1

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author name string

Giovanna Zorzi

2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Paola Venco

3

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Federica Zibordi

8

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Birgit Siegel

9

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Alessandro Simonati

11

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Nardo Nardocci

13

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

publication date

1 June 2012

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

number of pages

7

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based on heuristic

inferred from page(s)

Seminars in pediatric neurology

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

19

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

2

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

75-81

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

Identifiers

10.1016/J.SPEN.2012.03.006

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 February 2018

http://europepmc.org/abstract/MED/22704260

ResearchGate publication ID

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