Response by Roldan-Sevilla to Letter Regarding Article, "Missense Mutations in the FLNC Gene Causing Familial Restrictive Cardiomyopathy"

Circ Genom Precis Med. 2019 Jul;12(7):e002622. doi: 10.1161/CIRCGEN.119.002622. Epub 2019 Jul 15.

Authors

Álvaro Roldan-Sevilla¹, Rafael Salguero-Bodes^{1

2

3}, María Valverde-Gómez^{1

2

3}, Juan Delgado^{1

2

3}, Fernando Arribas-Ynsaurriaga^{1

2

3}, Julián Palomino-Doza^{1

2}

Affiliations

¹ Cardiology department, Hospital Universitario 12 de Octubre, Instituto de Investigación i+12 (Á.R.-S., R.S.-B., M.V.-G., J.D., F.A.-Y., J.P.-D.).
² Centro de Investigación Biomédica en Red en Enfermedades Cardiovasculares, CIBERCV (R.S.-B., M.V.-G., J.D., F.A.-Y., J.P.-D.).
³ Universidad Complutense de Madrid, Spain (R.S.-B., M.V.-G., J.D., F.A.-Y.).

PMID: 31306058
DOI: 10.1161/CIRCGEN.119.002622

No abstract available

Publication types

Letter
Comment

MeSH terms

Cardiomyopathy, Restrictive*
Filamins / genetics
Humans
Mutation, Missense
Pedigree

Substances

FLNC protein, human
Filamins