Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease (Q28235384)

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scientific article (publication date: 31 December 1991)
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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
scientific article (publication date: 31 December 1991)

    Statements

    Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease (English)
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    H Bujo
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    J Kusunoki
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    M Ogasawara
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    T Yamamoto
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    Y Ohta
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    T Shimada
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    Y Saito
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    S Yoshida
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    31 December 1991
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    181
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    3
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    933-40
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