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-Reference-Cited by-同舟云学术

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

Published:2015-06 Issue:6 Volume:208 Page:327-332
ISSN:2210-7762
Container-title:Cancer Genetics
language:en
Short-container-title:Cancer Genetics

Author:

Torres-Martín Miguel,Kusak M. Elena,Isla Alberto,Burbano Rommel R.,Pinto Giovanny R.,Melendez Barbara,Castresana Javier S.,Rey Juan A.

Funder

Fondo de Investigaciones Sanitarias

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

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