Wikidata

(Q54431143)

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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Statements

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

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