Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

about

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

Item

http://www.wikidata.org/entity/Q46123470

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh-hant

name

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@en

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@nl

type

Item

label

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@en

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@nl

prefLabel

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@en

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@nl

P1476

Double somatic SMARCB1 and NF2 mutations in sporadic spinal schwannoma.

@en

P2093

Anna Laura Putignano

http://www.w3.org/2001/XMLSchema#string

Gabriele Lorenzo Capone

http://www.w3.org/2001/XMLSchema#string

Irene Paganini

http://www.w3.org/2001/XMLSchema#string

Marco Giovannini

http://www.w3.org/2001/XMLSchema#string

Roberta Sestini

http://www.w3.org/2001/XMLSchema#string

P2860

Alteration in a new gene encoding a putative membrane-organizing protein causes neuro-fibromatosis type 2

Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers

Genomic analysis using high-density single nucleotide polymorphism-based oligonucleotide arrays and multiplex ligation-dependent probe amplification provides a comprehensive analysis of INI1/SMARCB1 in malignant rhabdoid tumors

Germline mutation of INI1/SMARCB1 in familial schwannomatosis

A method and server for predicting damaging missense mutations

The mouse ortholog of the human SMARCB1 gene encodes two splice forms

Evidence of a four-hit mechanism involving SMARCB1 and NF2 in schwannomatosis-associated schwannomas

Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome

MutationTaster evaluates disease-causing potential of sequence alterations

INI1 mutations in meningiomas at a potential hotspot in exon 9

P2888

s11060-017-2711-6

P304

33-38

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S11060-017-2711-6

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

137

http://www.w3.org/2001/XMLSchema#string

P50

Laura Papi

Jeremie Vitte

P577

2017-12-11T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

29230670

http://www.w3.org/2001/XMLSchema#string