(Q48595154)

English

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins.

scientific article published on 3 April 2006

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scholarly article

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

Disease severity in dominant Emery Dreifuss is increased by mutations in both emerin and desmin proteins. (English)

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

2

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

Aleksey Shatunov

10

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

12

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

author name string

F Muntoni

1

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

L G Goldfarb

3

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

E Mercuri

4

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

R J Piercy

5

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

M Burke

6

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

R Ben Yaou

7

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

P Richard

8

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

D Récan

9

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

C A Sewry

11

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

language of work or name

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publication date

3 April 2006

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

129

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

Pt 5

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

1260-1268

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

1 reference

24 May 2022

https://opencitations.net/index/coci/api/v1/citations/10.1038/NATURE01629

Identifiers

10.1093/BRAIN/AWL062

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

1 reference

Europe PubMed Central

13 February 2018

http://europepmc.org/abstract/MED/16585054

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