학술논문
A recurrent familial partial lipodystrophy due to a monoallelic or biallelic LMNA founder variant highlights the multifaceted cardiac manifestations of metabolic laminopathies
Document Type
Article
Author
Treiber, G.; Bonfanti, O.; Schneebeli, S.; Bernard, C.; Le-Moullec, N.; Pholsena, M.; Jarlet, E.; Domun, B.; Venault, A.; Venault, S.; Maiza, J.-C.; Cogne, M.; Nobécourt, E.; Furmaniuk, A.F.; Bakiri, F.; Guilleux, A.; Rollot, O.; Medjane, S.; Vatier, C.; Jéru, I.; Lascols, O.; Vigouroux, C.; Darcel, F.; Jacquemont, M.-L.; Doray, B.
Source
In: European Journal of Endocrinology . (European Journal of Endocrinology, October 2021, 185(4):453-462)
Subject
Language
English
ISSN
1479683X
08044643
08044643