X-linked methyl CpG binding protein (MeCP2) gene mutations in children with Rett syndrome: Correlation with clinical severity of gastrointestinal symptoms

被引：1
|
作者：
Cuffari, C
Darbari, A
Bibat, G
Naidu, S
机构：
来源：
GASTROENTEROLOGY | 2003年 / 124卷 / 04期
关键词：
D O I：
10.1016/S0016-5085(03)80202-0
中图分类号：
R57 [消化系及腹部疾病];
学科分类号：
摘要：
引用
收藏
页码：A41 / A41
页数：1
相关论文
共 50 条
  • [21] A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis
    Ma, D. Y.
    Li, G.
    Luo, C. Y.
    Liu, A.
    Zhang, J. J.
    Hu, P.
    Cheng, J.
    Wang, Y. G.
    Jiang, T.
    Xu, J. F.
    [J]. CLINICAL AND EXPERIMENTAL OBSTETRICS & GYNECOLOGY, 2018, 45 (06): : 924 - 929
  • [22] Role of DNA Methyl-CpG-Binding Protein MeCP2 in Rett Syndrome Pathobiology and Mechanism of Disease
    Pejhan, Shervin
    Rastegar, Mojgan
    [J]. BIOMOLECULES, 2021, 11 (01) : 1 - 27
  • [23] Mutations and polymorphisms in the human methyl CpG-binding protein MECP2
    Miltenberger-Miltenyi, G
    Laccone, F
    [J]. HUMAN MUTATION, 2003, 22 (02) : 107 - 115
  • [24] Mutation analysis of the methyl-CpG-binding protein 2 gene (MECP2) in Rett patients with preserved speech
    Yamashita, Y
    Kondo, I
    Fukuda, T
    Morishima, R
    Kusaga, A
    Iwanaga, R
    Matsuishi, T
    [J]. BRAIN & DEVELOPMENT, 2001, 23 : S157 - S160
  • [25] A mutation in the Rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
    Meloni, I
    Bruttini, M
    Longo, I
    Mari, F
    Rizzolio, F
    D'Adamo, P
    Denvriendt, K
    Fryns, JP
    Toniolo, D
    Renieri, A
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 67 (04) : 982 - 985
  • [26] Methyl-CpG-binding protein 2 mutations in Rett syndrome
    Van den Veyver, IB
    Zoghbi, HY
    [J]. CURRENT OPINION IN GENETICS & DEVELOPMENT, 2000, 10 (03) : 275 - 279
  • [27] Mutations in the gene encoding methyl-CpG-binding protein 2 cause Rett syndrome
    Van den Veyver, IB
    Zoghbi, HY
    [J]. BRAIN & DEVELOPMENT, 2001, 23 : S147 - S151
  • [28] Specific mutations in Methyl-CpG-Binding Protein 2 confer different severity in Rett syndrome
    Neul, J. L.
    Fang, P.
    Barrish, J.
    Lane, J.
    Caeg, E. B.
    Smith, E. O.
    Zoghbi, H.
    Percy, A.
    Glaze, D. G.
    [J]. NEUROLOGY, 2008, 70 (16) : 1313 - 1321
  • [29] X-linked gene expression and methylation in Rett syndrome: role of MeCP2 in epigenetic control of X chromosome inactivation.
    Carrel, L
    Chadwick, BP
    Trevarthen, KC
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) : 348 - 348
  • [30] Effects of Rett syndrome mutations of the methyl-CpG binding domain of the transcriptional repressor MeCP2 on selectivity for association with methylated DNA
    Ballestar, E
    Yusufzai, TM
    Wolffe, AP
    [J]. BIOCHEMISTRY, 2000, 39 (24) : 7100 - 7106
12345