(Q33800041)

29 July 2017

title

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis (English)

1 reference

29 July 2017

5

Sylviane Olschwang

1 reference

29 July 2017

Guillaume Rousseau

1

1 reference

29 July 2017

Tetsuro Noguchi

series ordinal

2

1 reference

29 July 2017

Violaine Bourdon

series ordinal

3

1 reference

29 July 2017

Hagay Sobol

series ordinal

4

1 reference

29 July 2017

publication date

24 January 2011

1 reference

29 July 2017

1 reference

29 July 2017

volume

11

1 reference

29 July 2017

page(s)

9

1 reference

Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3037869

The neurofibromatoses. Part 2: NF2 and schwannomatosis.

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3037869

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

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3037869

Germline mutation of INI1/SMARCB1 in familial schwannomatosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3037869

Diagnostic criteria for schwannomatosis

4 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3037869

Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype

4 July 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-9

Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-9

Schwannomatosis associated with multiple meningiomas due to a familial SMARCB1 mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-9

SMARCB1 mutations are not a common cause of multiple meningiomas

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-9

SMARCB1/INI1maternal germ line mosaicism in schwannomatosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-9

Alterations in the SMARCB1 (INI1) tumor suppressor gene in familial schwannomatosis

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21255467

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/21255467

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2377-11-9

1 reference

Dimensions Publication ID

29 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-11-9

9 September 2019

1 reference

29 July 2017

1 reference