Novel mutations in TARDBP (TDP-43) in patients with familial amyotrophic lateral sclerosis (Q28473603)

Jemeen Sreedharan

11

0 references

Dennis W. Dickson

Dennis W Dickson

28

0 references

Daniel Geschwind

16

Daniel H Geschwind

0 references

Christopher Shaw

Christopher E Shaw

22

0 references

Leonard Petrucelli

30

Leonard Petrucelli

0 references

Zbigniew K Wszolek

26

Zbigniew K Wszolek

0 references

Rosa Rademakers

31

Rosa Rademakers

0 references

Ronald C. Petersen

19

Ronald C Petersen

0 references

David S Knopman

17

David S Knopman

0 references

Hiroshi Mitsumoto

18

Hiroshi Mitsumoto

0 references

Bradley F Boeve

24

Bradley Boeve

0 references

Neil Cashman

20

Neil R Cashman

0 references

Neill R Graff-Radford

25

Neill R Graff-Radford

0 references

Kevin B Boylan

23

Kevin B Boylan

0 references

Karen M Kuntz

9

Karen Kuntz

0 references

Matt Baker

3

Matt Baker

0 references

Nicole A Finch

5

Nicole A Finch

0 references

Heather Ann Stewart

7

Heather Stewart

0 references

Brendan Kelley

8

Brendan J Kelley

0 references

Eric J Sorenson

13

Eric Sorenson

0 references

Carol F Lippa

14

Carol Lippa

0 references

Eileen H Bigio

15

Eileen H Bigio

0 references

author name string

Nicola J Rutherford

1

0 references

Yong-Jie Zhang

2

0 references

Jennifer M Gass

4

0 references

Ya-Fei Xu

6

0 references

Richard J P Crook

10

0 references

Mike Hutton

21

0 references

Richard J Caselli

27

0 references

Ian R Mackenzie

Creative Commons Attribution 4.0 International

29

0 references

language of work or name

English

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publication date

19 September 2008

0 references

published in

PLOS Genetics

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volume

4

0 references

issue

9

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page(s)

e1000193

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copyright license

start time

19 September 2008

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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19 March 2017

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19 March 2017

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19 March 2017

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Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

7 April 2017

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29 September 2017

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29 September 2017

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TDP-43 proteinopathies: neurodegenerative protein misfolding diseases without amyloidosis

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Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease.

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Identifiers

DOI

1 reference

253544

253544

1 reference

1 reference

1 reference