Reply to correspondence from Ogino et al. -: "Comment on SMN2 deletion in childhood-onset spinal muscular atrophy"

被引：0
|
作者：
Srivastava, S
Mukherjee, M
Panigrahi, I
Pandey, GS
Mittal, B [1 ]
Pradhan, S
机构：
[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Med Genet, Lucknow 226014, Uttar Pradesh, India
[2] Sanjay Gandhi Postgrad Inst Med Sci, Dept Neurol, Lucknow, Uttar Pradesh, India
来源：
AMERICAN JOURNAL OF MEDICAL GENETICS | 2002年 / 109卷 / 03期
关键词：
D O I：
10.1002/ajmg.10279
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：245 / 245
页数：1
相关论文
共 50 条
  • [11] A family with late-onset spinal muscular atrophy with remarkable phenotypic variability, influenced by SMN2 copy number
    Park, J. S.
    Kim, G. H.
    Kim, D. S.
    Shin, J. H.
    NEUROMUSCULAR DISORDERS, 2014, 24 (9-10) : 887 - 887
  • [12] Analysis of Deletions in SMN1, SMN2, and NAIPGenes in Spinal Muscular Atrophy Patients from the Northwestern Region of Russia
    A. S. Glotov
    A. V. Kiselev
    T. E. Ivaschenko
    V. S. Baranov
    Russian Journal of Genetics, 2001, 37 : 968 - 971
  • [13] Significant increase in the number of the SMN2 gene copies in an adult-onset type III spinal muscular atrophy patient with homozygous deletion of the NAIP gene
    Yamashita, M
    Nishio, H
    Harada, Y
    Matsuo, M
    Yamamoto, T
    EUROPEAN NEUROLOGY, 2004, 52 (02) : 101 - 106
  • [14] Analysis of deletions in SMN1, SMN2, and NAIP genes in spinal muscular atrophy patients from the northwestern region of Russia
    Glotov, AS
    Kiselev, AV
    Ivaschenko, TE
    Baranov, VS
    RUSSIAN JOURNAL OF GENETICS, 2001, 37 (08) : 968 - 971
  • [15] Rapid diagnosis of spinal muscular atrophy using tetra-primer ARMS PCR assay: Simultaneous detection of SMN1 and SMN2 deletion
    Baris, Ibrahim
    Etlik, Ozdal
    Koksal, Vedat
    Arican-Baris, S. Tugba
    MOLECULAR AND CELLULAR PROBES, 2010, 24 (03) : 138 - 141
  • [16] Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy: three SMN2 copies fail to rescue some patients from the disease severity
    Yosuke Harada
    Retno Sutomo
    Ahmad Hamim Sadewa
    Tomoko Akutsu
    Yasuhiro Takeshima
    Hiroko Wada
    Masafumi Matsuo
    Hisahide Nishio
    Journal of Neurology, 2002, 249 : 1211 - 1219
  • [17] Correlation between SMN2 copy number and clinical phenotype of spinal muscular atrophy:: three SMN2 copies fail to rescue some patients from the disease severity
    Harada, Y
    Sutomo, R
    Sadewa, AH
    Akutsu, T
    Takeshima, Y
    Wada, H
    Matsuo, M
    Nishio, H
    JOURNAL OF NEUROLOGY, 2002, 249 (09) : 1211 - 1219
  • [18] Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene
    Zarkov, Marija
    Stojadinovic, Aleksandra
    Sekulic, Slobodan
    Barjaktarovic, Iva
    Stojiljkovic, Olivera
    Peric, Stojan
    Kekovic, Goran
    Draskovic, Biljana
    Stevic, Zorica
    VOJNOSANITETSKI PREGLED, 2015, 72 (10) : 859 - 863
  • [19] Hyperacetylating agents activate SMN2 gene expression in fibroblast cultures from spinal muscular atrophy (SMA) patients
    Andreassi, C
    Tiziano, FD
    Angelozzi, C
    Vitali, T
    De Vincenzi, E
    Neri, G
    Brahe, C
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2002, 10 : 261 - 261
  • [20] Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the disease
    Jedrzejowska, Maria
    Milewski, Michal
    Zimowski, Janusz
    Borkowska, Janina
    Kostera-Pruszczyk, Anna
    Sielska, Danuta
    Jurek, Marta
    Hausmanowa-Petrusewicz, Irena
    ACTA BIOCHIMICA POLONICA, 2009, 56 (01) : 103 - 108
12345