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Congenital Generalized Lipodystrophy Type 1

Known as: Lipodystrophy, Congenital Generalized, Type 1, Berardinelli Seip Congenital Lipodystrophy Type 1, BRUNZELL SYNDROME, AGPAT2-RELATED 
It is caused by mutations of gene encoding 1-acylglycerol-3-phosphate O-acyltransferase-2 (AGPAT2).
National Institutes of Health

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2016
2016
CONTEXT Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive disorder characterized by near-total lack of… Expand
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Highly Cited
2003
Highly Cited
2003
Congenital generalized lipodystrophy (CGL) is a rare autosomal recessive syndrome characterized by extreme paucity of adipose… Expand
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Highly Cited
2002
Highly Cited
2002
Generalised lipodystrophy of the Berardinelli-Seip type (BSCL) is a rare autosomal recessive human disorder with severe adverse… Expand
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2002
2002
Abstract Frankenberg, D., Kelnhofer, K., Bär, K. and Frankenberg-Schwager, M. Enhanced Neoplastic Transformation by Mammography X… Expand
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Highly Cited
2001
Highly Cited
2001
Congenital generalized lipodystrophy, or Berardinelli–Seip syndrome (BSCL), is a rare autosomal recessive disease characterized… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract Lewis, D. A., Mayhugh, B. M., Qin, Y., Trott, K. and Mendonca, M. S. Production of Delayed Death and Neoplastic… Expand
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Highly Cited
2000
Highly Cited
2000
Fruiting body formation in the basidiomycete Coprinus cinereus is a developmental process that occurs as a response of the… Expand
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Highly Cited
1999
Highly Cited
1999
Congenital generalized lipodystrophy (CGL, Berardinelli-Seip Syndrome, OMIM # 269700) is a rare autosomal recessive disorder… Expand
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Highly Cited
1996
Highly Cited
1996
BACKGROUND Atopy is a common syndrome underlying asthma, rhinitis, and eczema, and is characterised by high immunoglobulin E (IgE… Expand
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1991
1991
Fusion of tumorigenic HeLa cells with human skin fibroblasts results in genetically stable hybrids which are nontumorigenic and… Expand
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