Open AccessDyslipemia in Familial Partial Lipodystrophy Caused by an R482W Mutation in the LMNA Gene
Author(s) -
H Schmidt
Publication year - 2001
Publication title -
the journal of clinical endocrinology and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.206
H-Index - 353
eISSN - 1945-7197
pISSN - 0021-972X
DOI - 10.1210/jc.86.5.2289
Subject(s) - lmna , hypertriglyceridemia , lipodystrophy , medicine , acanthosis nigricans , endocrinology , insulin resistance , missense mutation , diabetes mellitus , genetics , mutation , biology , triglyceride , immunology , gene , cholesterol , antiretroviral therapy , viral load , human immunodeficiency virus (hiv)
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