Reduced adipogenic gene expression in fibroblasts from a patient with type 2 congenital generalized lipodystrophy

Author:

Victoria B.,Cabezas-Agrícola J. M.,González-Méndez B.,Lattanzi G.,Del Coco R.,Loidi L.,Barreiro F.,Calvo C.,Lado-Abeal J.,Araújo-Vilar D.

Publisher

Wiley

Subject

Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference49 articles.

1. Phenotypic and genetic heterogeneity in congenital generalized lipodystrophy;Agarwal;J Clin Endocrinol Metab,2003

2. General lipodystrophy, congenital and acquired (lipoatrophy);Seip;Acta Paediatr,1996

3. Studies of insulin resistance in congenital generalized lipodystrophy;Sovik;Acta Paediatr,1996

4. Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects;Fu;J Clin Endocrinol Metab,2004

5. Leptin levels, β-cell function, and insulin sensitivity in families with congenital and acquired generalized lipoatropic diabetes;Pardini;J Clin Endocrinol Metab,1998

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