Group:MUZIC:FilaminC: Difference between revisions

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	• A mutation of 577G---->A (Ala193Thr)in the Filamin C ABD has been shown to cause dominant distal myopathy <ref> PMID 21620354 </ref>		• A mutation of 577G---->A (Ala193Thr)in the Filamin C ABD has been shown to cause dominant distal myopathy <ref> PMID 21620354 </ref>

	For an extended pathophysiology of the MFM, see <ref> PMID 22961544 </ref>		For an extended pathophysiology of the MFM, see <ref> PMID 22961544 </ref> <ref> PMID 23109048 </ref>