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A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome
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A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndrome

C Albrecht, JH McVey, JI Elliott, A Sardini, I Kasza, AD Mumford, RP Naoumova, EGD Tuddenham, K Szabo and CF Higgins
BLOOD, Vol.106(2), pp.542-549
15/07/2005

Abstract

Science & Technology Life Sciences & Biomedicine Hematology HEMATOLOGY BINDING CASSETTE TRANSPORTER DENSITY-LIPOPROTEIN DEFICIENCY HUMAN MULTIDRUG TRANSPORTER TANGIER-DISEASE CHOLESTEROL EFFLUX GENE-TRANSFER TRANSMEMBRANE MIGRATION MEMBRANE PHOSPHOLIPIDS INHERITED DISORDER APOPTOTIC CELLS
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