Characterisation of non-obese diabetic patients with marked insulin resistance identifies a novel familial partial lipodystrophy-associated PPARγ mutation (Y151C)

AIMS/HYPOTHESIS: Familial partial lipodystrophy (FPLD) is a rare metabolic disorder with clinical features that may not be readily recognised. As FPLD patients require a specific therapeutic approach, early identification is warranted. In the present study we aimed to identify cases of FPLD among no...

Descripción completa

Detalles Bibliográficos
Autores principales: Visser, M. E., Kropman, E., Kranendonk, M. E., Koppen, A., Hamers, N., Stroes, E. S., Kalkhoven, E., Monajemi, H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
Materias:
Short Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110271/
https://www.ncbi.nlm.nih.gov/pubmed/21479595
http://dx.doi.org/10.1007/s00125-011-2142-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110271/
https://www.ncbi.nlm.nih.gov/pubmed/21479595
http://dx.doi.org/10.1007/s00125-011-2142-4

Ejemplares similares