NOVEL RAC2 MUTATION AS THE MOLECULAR CAUSE OF HEREDITARY HEMOLYTIC ANEMIA

被引：0
|
作者：
Glasser, Chana
Weinblatt, Mark
Emberesh, Myesa
Konstantinidis, Diamantis
Ottlinger, Anna
Kalfa, Theodosia
机构：
[1] NYU, Winthrop Hosp, Mineola, NY USA
[2] NYU, Winthrop Hosp, Cincinnati, OH USA
[3] Cincinnati Childrens Hosp Med Ctr, Mineola, NY USA
[4] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH 45229 USA
来源：
PEDIATRIC BLOOD & CANCER | 2020年 / 67卷
关键词：
D O I：
暂无
中图分类号：
R73 [肿瘤学];
学科分类号：
100214 ;
摘要：
142
引用
收藏
页码：S51 / S51
页数：1
相关论文
共 50 条
  • [21] Molecular basis for Rac2 regulation of phagocyte NADPH oxidase
    Becky A. Diebold
    Gary M. Bokoch
    Nature Immunology, 2001, 2 : 211 - 215
  • [22] Molecular basis for Rac2 regulation of phagocyte NADPH oxidase
    Diebold, BA
    Bokoch, GM
    NATURE IMMUNOLOGY, 2001, 2 (03) : 211 - 215
  • [23] A Novel RAC2 Variant Presenting as Severe Combined Immunodeficiency
    Heather Stern
    Agnes Donkó
    Teresa Shapiro
    Amy P. Hsu
    Thomas L. Leto
    Steven M. Holland
    Doerthe Adriana Andreae
    Journal of Clinical Immunology, 2021, 41 : 473 - 476
  • [24] A Novel RAC2 Variant Presenting as Severe Combined Immunodeficiency
    Stern, Heather
    Donko, Agnes
    Shapiro, Teresa
    Hsu, Amy P.
    Leto, Thomas L.
    Holland, Steven M.
    Andreae, Doerthe Adriana
    JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (02) : 473 - 476
  • [25] GAMMA-GLUTAMYL-CYSTEINE SYNTHETASE DEFICIENCY - CAUSE OF HEREDITARY HEMOLYTIC ANEMIA
    KONRAD, PN
    VALENTINE, WN
    PAGLIA, DE
    RICHARDS, F
    NEW ENGLAND JOURNAL OF MEDICINE, 1972, 286 (11): : 557 - +
  • [26] HEREDITARY HEMOLYTIC ANEMIA DUE TO RED CELL MONOVALENT CATION LEAK IN A PATIENT WITH A NOVEL BAND 3 MUTATION
    Gupta, Shveta
    Baskin, Jacquelyn
    Kalfa, Theodosia
    Risinger, Mary
    Zhang, Kejian
    PEDIATRIC BLOOD & CANCER, 2016, 63 : S58 - S59
  • [27] GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY - NEW CAUSE OF HEREDITARY HEMOLYTIC ANEMIA
    KONRAD, PN
    RICHARDS, F
    VALENTIN.WN
    PAGLIA, DE
    BLOOD-THE JOURNAL OF HEMATOLOGY, 1971, 38 (06): : 808 - &
  • [28] A novel mutation in the human red cell type pyruvate kinase gene causing hereditary nonspherocytic hemolytic anemia
    vanSolinge, WW
    Nielsen, FC
    vanWijk, R
    BruunPetersen, G
    WiltonDjernes, B
    Kraaijenhagen, RJ
    Rijksen, G
    BRITISH JOURNAL OF HAEMATOLOGY, 1996, 93 : 569 - 569
  • [29] Clinical features of a human Rac2 mutation: A complex neutrophil dysfunction disease
    Kurkchubasche, AG
    Panepinto, JA
    Tracy, TF
    Thurman, GW
    Ambruso, DR
    JOURNAL OF PEDIATRICS, 2001, 139 (01): : 141 - 147
  • [30] HEMOGLOBIN GRAND JUNCTION: A NOVEL MUTATION ASSOCIATED WITH HEMOLYTIC ANEMIA
    Kent, Michael
    Breaux, Charles, Jr.
    Oliveira, Jennifer
    Liang, Xiayuan
    Hoyer, James
    Swanson, Kenneth
    Silliman, Christopher
    PEDIATRIC BLOOD & CANCER, 2012, 58 (07) : 1074 - 1075
12345