This website provides information on patients with mutations in the ASNA1 gene, including clinical data, molecular data, management and research options.

Mutations in the ASNA1 gene (also referred to as GET3; OMIM: 601913) cause a rapidly progressive cardiomyopathy resulting in acute heart failure and death in early infancy.

This website was created to share and collect information about clinic, management and research projects to gather more knowledge and provide better treatment of patients with mutations in the ASNA1 gene.

Judith M.A. Verhagen, MD, PhD, Erasmus University Medical Center, Rotterdam, the Netherlands, j.m.a.verhagen@erasmusmc.nl

Ingrid M.B.H. van de Laar, MD, PhD, Erasmus University Medical Center, Rotterdam, the Netherlands, i.vandelaar@erasmusmc.nl