Novel mutations in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia

Novel mutations in the microsomal triglyceride transfer protein gene causing abetalipoproteinemia

Abetalipoproteinemia (ABL) is an inherited disease characterized by the virtual absence of apolipoprotein B (apoB)-containing lipoproteins from plasma. Only limited numbers of families have been screened for mutations in the microsomal triglyceride transfer protein (MTP) gene. To clarify the genetic...

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Bibliographic Details
Main Authors:	Ken Ohashi, Shun Ishibashi, Jun-ichi Osuga, Ryu-ichi Tozawa, Kenji Harada, Naoya Yahagi, Futoshi Shionoiri, Yoko Iizuka, Yoshiaki Tamura, Ryozo Nagai, D. Roger Illingworth, Takanari Gotoda, Nobuhiro Yamada
Format:	Article
Language:	English
Published:	Elsevier 2000-08-01
Series:	Journal of Lipid Research
Subjects:	microsomal triglyceride transfer protein abetalipoproteinemia apolipoprotein B triglycerides cholesterol lipoproteins
Online Access:	http://www.sciencedirect.com/science/article/pii/S002222752033426X

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