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                                       Details for article 7 of 20 found articles
 
 
  An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains
 
 
Title: An Autosomal Dominant Cerebellar Ataxia Linked to Chromosome 16q22.1 Is Associated with a Single-Nucleotide Substitution in the 5′ Untranslated Region of the Gene Encoding a Protein with Spectrin Repeat and Rho Guanine-Nucleotide Exchange-Factor Domains
Author: Ishikawa, Kinya
Toru, Shuta
Tsunemi, Taiji
Li, Mingshun
Kobayashi, Kazuhiro
Yokota, Takanori
Amino, Takeshi
Owada, Kiyoshi
Fujigasaki, Hiroto
Sakamoto, Masaki
Tomimitsu, Hiroyuki
Takashima, Minoru
Kumagai, Jiro
Noguchi, Yoshihiro
Kawashima, Yoshiyuki
Ohkoshi, Norio
Ishida, Gen
Gomyoda, Manabu
Yoshida, Mari
Hashizume, Yoshio
Saito, Yuko
Murayama, Shigeo
Yamanouchi, Hiroshi
Mizutani, Toshio
Kondo, Ikuko
Toda, Tatsushi
Mizusawa, Hidehiro
Appeared in: The American journal of human genetics
Paging: Volume 77 (2005) nr. 2 pages 17 p.
Year: 2005
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 20 found articles
 
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