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Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature

✍ Scribed by Bijan Roshan; Om P. Ganda; Ranil DeSilva; Rose B. Ganim; Edmund Ward; Sarah D. Haessler; Eliana Y. Polisecki; Bela F. Asztalos; Ernst J. Schaefer


Book ID
119288076
Publisher
Elsevier
Year
2011
Tongue
English
Weight
429 KB
Volume
5
Category
Article
ISSN
1933-2874

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