학술논문
A case of Dunnigan-type familial partial lipodystrophy (FPLD) due to lamin A/C (LMNA) mutations complicated by end-stage renal disease
Document Type
Article
Author
Source
In: Endocrine . (Endocrine, February 2009, 35(1):18-21)
Subject
Language
English
ISSN
1355008X