Peroxisomal proliferator activated receptor-γ deficiency in a Canadian kindred with familial partial lipodystrophy type 3 (FPLD3)
<p>Abstract</p> <p>Background</p> <p>Familial partial lipodystrophy (Dunnigan) type 3 (FPLD3, Mendelian Inheritance in Man [MIM] 604367) results from heterozygous mutations in <it>PPARG </it>encoding peroxisomal proliferator-activated receptor-γ. Both domina...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2006-01-01
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Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/7/3 |