SUN-556 Cardiac Phenotype in Familial Partial Lipodystrophy

Background Pathogenic variants in Lamin A/C (LMNA) gene are the most common monogenic etiology in Familial Partial Lipodystrophy (FPLD) causing FPLD2. LMNA pathogenic variants have been previously associated with cardiomyopathy, familial arrhythmias or conduction system abnormalities independent of...

Descripción completa

Detalles Bibliográficos
Autores principales: Eldin, Abdelwahab Jalal, Akinci, Baris, da Rocha, Andre Monteiro, Meral, Rasimcan, Simsir, Ilgin Yildirim, Adiyaman, Suleyman Cem, Ozpelit, Ebru, Bhave, Nicole, Gen, Ramazan, Yurekli, Banu Sarer, Kutbay, Nilufer Ozdemir, Siklar, Zeynep, Neidert, Adam, Swaidan, Mario, Rus, Diana, Hench, Rita, Jalife, Jose, Oral, Hakan, Oral, Elif A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Cardiovascular Endocrinology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207313/
http://dx.doi.org/10.1210/jendso/bvaa046.1116

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7207313/
http://dx.doi.org/10.1210/jendso/bvaa046.1116

Ejemplares similares