[HTML][HTML] Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary Deficiency of Microsomal Triglyceride Transfer Protein in Human Abetalipoproteinemia Is Associated with Loss of CD1 Function
S Zeissig, SK Dougan, DC Barral, Y Junker… - Journal of Clincial …, 2010 - ir.lib.uwo.ca
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
S Zeissig, SK Dougan, DC Barral… - Journal of Clinical …, 2010 - research.manchester.ac.uk
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function.
S Zeissig, S Dougan, D Barral, Y Junker… - Journal of clinical …, 2010 - ora.ox.ac.uk
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
S Zeissig, SK Dougan, DC Barral… - Journal of Clinical …, 2010 - search.proquest.com
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
[HTML][HTML] Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
S Zeissig, SK Dougan, DC Barral, Y Junker… - The Journal of …, 2010 - ncbi.nlm.nih.gov
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
S Zeissig, SK Dougan, DC Barral… - Journal of Clinical …, 2010 - research.birmingham.ac.uk
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
SM Kennedy, NO Davidson, S Zeissig, SK Dougan… - 2010 - digitalcommons.wustl.edu
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function
S Zeissig, SK Dougan, DC Barral… - Journal of Clinical …, 2010 - profiles.wustl.edu
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
Primary deficiency of microsomal triglyceride transfer protein in human abetalipoproteinemia is associated with loss of CD1 function.
S Zeissig, SK Dougan, DC Barral, Y Junker… - 1558 …, 2010 - escholar.manchester.ac.uk
Abetalipoproteinemia (ABL) is a rare Mendelian disorder of lipid metabolism due to genetic
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …
deficiency in microsomal triglyceride transfer protein (MTP). It is associated with defects in …