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
- 1 June 2010
- journal article
- research article
- Published by Elsevier BV in Neuromuscular Disorders
- Vol. 20 (6), 390-396
- https://doi.org/10.1016/j.nmd.2010.03.009
Abstract
No abstract availableKeywords
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