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  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
 
 
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
Author: Luan, Xinghua
Hong, Daojun
Zhang, Wei
Wang, Zhaoxia
Yuan, Yun
Appeared in: Neuromuscular disorders
Paging: Volume 20 (2010) nr. 6 pages 7 p.
Year: 2010
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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