A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family. (Q54431143)

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scientific article published on 22 April 2010

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English	A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family.	scientific article published on 22 April 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

title

A novel heterozygous deletion-insertion mutation (2695-2712 del/GTTTGT ins) in exon 18 of the filamin C gene causes filaminopathy in a large Chinese family. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

main subject

heterozygosity

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based on heuristic

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author name string

Xinghua Luan

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1

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Europe PubMed Central

PubMed publication ID

20417099

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29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

Daojun Hong

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2

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Europe PubMed Central

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20417099

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29 May 2018

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http://europepmc.org/abstract/MED/20417099

Wei Zhang

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3

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Europe PubMed Central

PubMed publication ID

20417099

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29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

Zhaoxia Wang

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4

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PubMed publication ID

20417099

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29 May 2018

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http://europepmc.org/abstract/MED/20417099

Yun Yuan

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5

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Europe PubMed Central

PubMed publication ID

20417099

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29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

publication date

22 April 2010

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20417099

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29 May 2018

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http://europepmc.org/abstract/MED/20417099

published in

Neuromuscular Disorders

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Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

volume

20

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Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

issue

6

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Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

page(s)

390-396

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Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

Identifiers

DOI

10.1016/J.NMD.2010.03.009

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

PubMed publication ID

20417099

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20417099

retrieved

29 May 2018

reference URL

http://europepmc.org/abstract/MED/20417099

 

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