Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS). (Q33749062)

29 July 2017

title

Mutations in CHMP2B in lower motor neuron predominant amyotrophic lateral sclerosis (ALS). (English)

1 reference

amyotrophic lateral sclerosis

29 July 2017

main subject

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Emily F Goodall

3

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Heather Mortiboys

Heather Mortiboys

6

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Laura Ferraiuolo

Laura Ferraiuolo

2

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Andrew Grierson

Andrew J Grierson

13

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Janine Kirby

Janine Kirby

15

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Paul Ince

Paul G Ince

14

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Pamela Shaw

Pamela J Shaw

16

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author name string

Laura E Cox

1

1 reference

29 July 2017

Paul R Heath

4

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29 July 2017

Adrian Higginbottom

5

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29 July 2017

Hannah C Hollinger

7

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29 July 2017

Judith A Hartley

8

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29 July 2017

Alice Brockington

9

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29 July 2017

Christine E Burness

10

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29 July 2017

Karen E Morrison

11

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29 July 2017

Stephen B Wharton

12

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29 July 2017

language of work or name

English

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publication date

24 March 2010

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29 July 2017

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29 July 2017

volume

5

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29 July 2017

issue

3

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29 July 2017

page(s)

e9872

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Creative Commons Attribution 4.0 International

29 July 2017

copyright license

start time

24 March 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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describes a project that uses

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2844426/fullTextXML

inferred from PubMed Central ID database lookup

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21 June 2018

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30 October 2018

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30 October 2018

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Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

30 October 2018

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Motor neuron disease in a patient with a mitochondrial tRNAIle mutation

30 October 2018

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30 October 2018

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30 October 2018

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30 October 2018

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The Rab5 Activator ALS2/alsin Acts as a Novel Rac1 Effector through Rac1-activated Endocytosis

30 October 2018

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Large-scale SOD1 mutation screening provides evidence for genetic heterogeneity in amyotrophic lateral sclerosis

10 December 2018

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12 December 2020

Erratum: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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12 December 2020

Identification of a novel exon 4 SOD1 mutation in a sporadic amyotrophic lateral sclerosis patient

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12 December 2020

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

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12 December 2020

CHMP2B mutations are not a common cause of familial or sporadic amyotrophic lateral sclerosis

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12 December 2020

Genetics of amyotrophic lateral sclerosis

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12 December 2020

10.1371/JOURNAL.PONE.0009872

Identifiers

DOI

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29 July 2017

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29 July 2017

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