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...

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Detaylı Bibliyografya
Yayımlandı:J Endocr Soc
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2020
Konular:
Cardiovascular Endocrinology
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7207313/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1210/jendso/bvaa046.1116
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