filamin-C isoform X3 [Rattus norvegicus]

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Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy. [Nat Commun. 2014]
Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy.
Valdés-Mas R, Gutiérrez-Fernández A, Gómez J, Coto E, Astudillo A, Puente DA, Reguero JR, Álvarez V, Morís C, León D, et al. Nat Commun. 2014 Oct 29; 5:5326. Epub 2014 Oct 29.
Structural basis for vertebrate filamin dimerization. [Structure. 2005]
Structural basis for vertebrate filamin dimerization.
Pudas R, Kiema TR, Butler PJ, Stewart M, Ylänne J. Structure. 2005 Jan; 13(1):111-9.
Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure. [Mol Cell Biol. 2006]
Loss of FilaminC (FLNc) results in severe defects in myogenesis and myotube structure.
Dalkilic I, Schienda J, Thompson TG, Kunkel LM. Mol Cell Biol. 2006 Sep; 26(17):6522-34.

RefSeq mRNA
See reference mRNA sequence for the Flnc gene (XM_006236214.5).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Flnc gene.

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GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
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