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Familial Partial Lipodystrophy, Type 3

Known as: FPLD3, Lipodystrophy, Familial Partial, Associated With PPARg Mutations, Lipodystrophy, Familial Partial, Type 3 
This type can be caused by mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.
National Institutes of Health

Papers overview

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2019
2019
Latar belakang : Obesitas menjadi epidemik global saat ini. Masyarakat ini mulai menggunakan diet ketogenik yang rendah… 
2015
2015
We investigated whether Pro12Ala (C→G) and His447His (C→T) polymorphisms of the peroxisome proliferatoractivated receptor gamma… 
2012
2012
1 Background: The peroxisome proliferator activated receptors (PPARs) are transcriptional 2 regulators of lipid metabolism… 
2008
2008
Background.The correlation of gene variants with biological variables or clinical assessments has not been well understood… 
Review
2008
Review
2008
Stephane Cauchi (Stephane.Cauchi@good.ibl.fr) Kevin T Nead (knuf08@ufl.edu) Helene Choquet (helene@good.ibl.fr) Fritz Horber… 
2005
2005
Human lipodystrophies represent a group of diseases characterized by altered body fat amount and/or repartition and major…