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Molecular defect in familial lecithin:Cholesterol acyltransferase (LCAT) deficiency: A single nucleotide insertion in LCAT gene causes a complete deficient type of the disease

✍ Scribed by Hideaki Bujo; Jun Kusunoki; Masahito Ogasawara; Tokuo Yamamoto; Yoshiaki Ohta; Toshisune Shimada; Yasushi Saito; Sho Yoshida

Book ID: 115764741
Publisher: Elsevier Science
Year: 1991
Tongue: English
Weight: 702 KB
Volume: 181
Category: Article
ISSN: 0006-291X
DOI: 10.1016/0006-291x(91)92026-g

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