- ►diabetesjournals.org KR Owen, CJ Groves, RL Hanson, WC Knowler, … - Diabetes, 2007 - Am Diabetes Assoc Mutations in the LMNA gene (encoding lamin A/C) underlie familial partial
lipodystrophy, a syndrome of monogenic insulin resistance and diabetes. LMNA
maps to the well-replicated diabetes-linkage region on chromosome 1q, and ... Cited by 12 - Related articles - BL Direct - All 9 versions
P Lahiry, RL Pollex, RA Hegele - Journal of Nutrigenetics and Nutrigenomics, 2008 - content.karger.com The metabolic syndrome (MetS) is a commonly encountered cluster of clinical
phenotypes, including central obesity, hypertension, hyperglycemia, and
dyslipidemia. Identifying genetic determinants of MetS will lead to better ... Cited by 2 - Related articles - BL Direct - All 4 versions
K Duesing, G Charpentier, M Marre, J Tichet, … - Diabetologia, 2008 - Springer Page 1. ARTICLE Evaluating the association of common LMNA variants with type 2 diabetes
and quantitative metabolic phenotypes in French Europids ... Cited by 1 - Related articles - BL Direct - All 2 versions
B Fontaine-Bisson, MC Alessi, N Saut, F … - Journal of Molecular Medicine - Springer Abstract Laminopathies are rare monogenic diseases, some of them exhibiting
features of the metabolic syndrome. These diseases are mainly due to mutations
in LMNA, encoding A-type lamins. One LMNA polymor- phism, rs4641, has been ... Related articles - All 2 versions
- ►diabetesjournals.org KR Owen, CJ Groves, RL Hanson, WC Knowler, … - Diabetes, 2007 - Am Diabetes Assoc Mutations in the LMNA gene (encoding lamin A/C) underlie familial partial
lipodystrophy, a syndrome of monogenic insulin resistance and diabetes. LMNA
maps to the well-replicated diabetes-linkage region on chromosome 1q, and ... Related articles - All 3 versions