A novel non-truncating ApoB gene mutation, R463W, causes familial hypobetalipoproteinemia

被引:0
|
作者
Burnett, JR
Shan, J
Miskie, BA
Hooper, AJ
Yuan, J
Tran, K
Yao, Z
Hegele, RA
机构
[1] Univ Western Australia, Perth, WA 6009, Australia
[2] Univ Ottawa, Inst Heart, Ottawa, ON, Canada
[3] Robarts Res Inst, London, ON N6A 5C1, Canada
关键词
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
1260
引用
收藏
页码:251 / 251
页数:1
相关论文
共 50 条
  • [1] A novel non-truncating APOB gene mutation, R463W, causes familial hypobetalipoproteinaemia
    Burnett, JR
    Shan, J
    Miskie, BA
    Whitfield, AJ
    Yuan, J
    Tran, K
    Mcknight, CJ
    Yao, Z
    Hegele, RA
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (5-6) : A13 - A13
  • [2] A novel nontruncating APOB gene mutation, R463W, causes familial hypobetalipoproteinemia
    Burnett, JR
    Shan, J
    Miskie, BA
    Whitfield, AJ
    Yuan, J
    Tran, K
    McKnight, CJ
    Hegele, RA
    Yao, ZM
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (15) : 13442 - 13452
  • [3] A novel non-truncating APOB gene mutation, L343V, causes familial hypobetalipoproteinaemia
    Whitfield, A
    Crawford, G
    Robertson, K
    Barrett, P
    Hegele, R
    Tran, K
    Yao, Z
    van Bockxmeer, F
    Burnett, J
    ATHEROSCLEROSIS SUPPLEMENTS, 2004, 5 (01) : 78 - 79
  • [4] Familial hypobetalipoproteinemia due to apolipoprotein B R463W mutation causes intestinal fat accumulation and low postprandial lipemia
    Noto, Davide
    Cefalu, Angelo B.
    Cannizzaro, Alessandra
    Mina, Mariangela
    Fayer, Francesca
    Valenti, Vincenza
    Barbagallo, Carlo M.
    Tuttolomondo, Antonino
    Pinto, Antonio
    Sciume, Carmelo
    Licata, Giuseppe
    Averna, Maurizio
    ATHEROSCLEROSIS, 2009, 206 (01) : 193 - 198
  • [5] Novel APOB mutation in familial hypobetalipoproteinemia
    Domenech, M.
    Llano-Rivas, Isabel
    Arroyo, Vicente
    Ortega, Emilio
    JOURNAL OF CLINICAL LIPIDOLOGY, 2022, 16 (01) : 28 - 32
  • [6] A novel nontruncating APOB gene mutation, L343V, causes familial hypobetalipoproteinemia
    Whitfield, AJ
    Crawford, G
    Barrett, PH
    Robertson, K
    Hegele, RA
    Tran, K
    Yao, ZM
    van Bockxmeer, FM
    Burnett, JR
    ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2004, 24 (05) : E55 - E55
  • [7] A novel truncating APOB gene mutation, apoB-40.3, causing familial hypobetalipoproteinaemia
    Whitfield, AJ
    Robertson, K
    Barrett, PHR
    Van Bockxmeer, FM
    Burnett, JR
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (5-6) : A25 - A25
  • [8] Familial hypobetalipoproteinemia: Clinical characterization of a new mutation in the APOB gene
    Iglesias, Pedro
    Diez, Juan J.
    Tarugi, Patrizia
    MEDICINA CLINICA, 2009, 133 (02): : 57 - 60
  • [9] Novel mutation (c.G1124A) in Exon 9 of the APOB gene causes aberrant splicing and familial hypobetalipoproteinemia
    Homer, Vivienne M.
    George, Peter M.
    CLINICAL CHEMISTRY, 2007, 53 (06) : 1165 - 1167
  • [10] A Rare Mutation in The APOB Gene Associated with Neurological Manifestations in Familial Hypobetalipoproteinemia
    Musialik, Joanna
    Boguszewska-Chachulska, Anna
    Pojda-Wilczek, Dorota
    Gorzkowska, Agnieszka
    Szymanczak, Robert
    Kania, Magdalena
    Kujawa-Szewieczek, Agata
    Wojcieszyn, Malgorzata
    Hartleb, Marek
    Wiecek, Andrzej
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (04)