(Q40931810)

English

Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules.

scientific article published on 11 April 2015

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25981829%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

Whole exome sequencing in a case of sporadic multiple meningioma reveals shared NF2, FAM109B, and TPRXL mutations, together with unique SMARCB1 alterations in a subset of tumor nodules (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25981829%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

Javier S. Castresana

7

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8 March 2020

Miguel Torres-Martín

1

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8 March 2020

Giovanny R Pinto

5

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8 March 2020

Barbara Melendez

6

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8 March 2020

author name string

M Elena Kusak

2

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8 March 2020

Alberto Isla

3

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8 March 2020

Rommel R Burbano

4

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8 March 2020

Juan A Rey

8

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8 March 2020

publication date

11 April 2015

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8 March 2020

Cancer Genetics

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8 March 2020

208

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8 March 2020

6

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8 March 2020

327-332

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8 March 2020

Identifiers

10.1016/J.CANCERGEN.2015.03.012

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8 March 2020

1 reference

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8 March 2020

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