Response by Ma et al to Letter Regarding Article, "Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy"

Circ Genom Precis Med. 2018 Apr;11(4):e002140. doi: 10.1161/CIRCGEN.118.002140.

Authors

Nathan R Tucker¹, Patrick T Ellinor¹

Affiliation

¹ Cardiovascular Research Center, Massachusetts General Hospital, Boston (N.R.T., P.T.E.); and Program in Medical and Population Genetics, The Broad Institute of MIT and Harvard, Cambridge, MA (N.R.T., P.T.E.).

PMID: 29650770
DOI: 10.1161/CIRCGEN.118.002140

No abstract available

Publication types

Letter
Comment

MeSH terms

Cardiomyopathy, Restrictive*
Filamins / genetics*
Humans
Mutation
Pedigree

Substances

FLNC protein, human
Filamins