Volume 13. ABCA1 Deficiency: A Disease of “Impaired Active Raft Disruption”
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ABCA1 Deficiency: A Disease of “Impaired Active Raft Disruption”
Description
A unified mechanism for any human disease is proposed in this book series based on abnormal membrane microdomain phenotypes. Membrane microdomain phenotypes induced by primary loss or secondary inactivation of ABCA1, one of the most important active raft disruptors in the human body, is discussed in this volume.
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