Novel nonsense mutation in exon 15 of the APC gene in one Jewish family

被引:0
|
作者
Monakov, O
Shemesh, E
Bar-Meir, S
Gazit, E [1 ]
机构
[1] Chaim Sheba Med Ctr, Tissue Typing Lab, IL-52621 Ramat Gan, Israel
[2] Chaim Sheba Med Ctr, Dept Gastroenterol, IL-52621 Ramat Gan, Israel
关键词
D O I
暂无
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
引用
收藏
页码:S55 / S55
页数:1
相关论文
共 50 条
  • [1] A silent mutation in exon 14 of the APC gene is associated with exon skipping in a FAP family
    Montera, M
    Piaggio, F
    Marchese, C
    Gismondi, V
    Stella, A
    Resta, N
    Varesco, L
    Guanti, G
    Mareni, C
    JOURNAL OF MEDICAL GENETICS, 2001, 38 (12) : 863 - 867
  • [2] Report on mutation in exon 15 of the APC gene in a case of brain metastasis
    Pecina-Slaus, Nives
    Majic, Zeljka
    Musani, Vesna
    Zeljko, Martina
    Cupic, Hrvoje
    JOURNAL OF NEURO-ONCOLOGY, 2010, 97 (01) : 143 - 148
  • [3] Report on mutation in exon 15 of the APC gene in a case of brain metastasis
    Nives Pećina-Šlaus
    Željka Majić
    Vesna Musani
    Martina Zeljko
    Hrvoje Čupić
    Journal of Neuro-Oncology, 2010, 97 : 143 - 148
  • [4] A novel frameshift mutation in the APC gene at exon 15 in familial adenomatous polyposis (FAP) with desmoid tumour
    Ekwueme, Kingsley C.
    McCarthy, Emma
    Healey, Claire
    Ellis, Anthony
    Rooney, Paul S.
    SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 2007, 42 (06) : 788 - 790
  • [5] A Novel Nonsense Mutation in Exon 5 of KIND1 Gene in an Iranian Family with Kindler Syndrome
    Heidari, Mohammad Mehdi
    Khatami, Mehri
    Kargar, Saeed
    Azari, Mojdeh
    Hoseinzadeh, Hassan
    Fallah, Hamedeh
    ARCHIVES OF IRANIAN MEDICINE, 2016, 19 (06) : 403 - 408
  • [6] A nonsense mutation in exon 8 of the APC gene (Arg283Ter) causes clinically variable FAP in a Malaysian Chinese family
    Mohamed, Z
    Ahmad, R
    Yoke, NS
    Zakaria, Z
    Ahmad, H
    Yew, TH
    CANCER SCIENCE, 2003, 94 (08) : 725 - 728
  • [7] A Novel Germline Mutation in Exon 15 of the APC Gene in Attenuated Familial Adenomatous Polyposis: A Report of Two Cases
    Jahng, Jaehoon
    Yoon, Sang Jin
    Park, Hyojin
    GUT AND LIVER, 2013, 7 (01) : 120 - 125
  • [8] A novel nonsense mutation of the sedlin gene in a family with spondyloepiphyseal dysplasia tarda
    Shi, YR
    Lee, CC
    Hsu, YA
    Wang, CH
    Tsai, FJ
    HUMAN HEREDITY, 2002, 54 (01) : 54 - 56
  • [9] A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia
    Wu, SY
    Wang, ZY
    Dong, NZ
    Bai, X
    Ruan, CG
    BLOOD COAGULATION & FIBRINOLYSIS, 2005, 16 (03) : 221 - 226
  • [10] A novel nonsense mutation in the NDP gene in a Chinese family with Norrie disease
    Liu, Deyuan
    Hu, Zhengmao
    Peng, Yu
    Yu, Changhong
    Liu, Yalan
    Mo, Xiaoyun
    Li, Xiaoping
    Lu, Lina
    Xu, Xiaojuan
    Su, Wei
    Pan, Qian
    Xia, Kun
    MOLECULAR VISION, 2010, 16 (280-84): : 2653 - 2658