Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature by Roshan, Bijan, MD, Ganda, Om P., MD, DeSilva, Ranil, MD, Ganim, Rose B., MD, Ward, Edmund, JD, Haessler, Sarah D., MD, Polisecki, Eliana Y., PhD, Asztalos, Bela F., PhD, Schaefer, Ernst J., MD

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