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                                       Details for article 5 of 71 found articles
 
 
  A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
 
 
Title: A homozygous structural variant of RPGRIP1 is frequently associated with achromatopsia in Japanese patients with IRD
Author: Suga, Akiko
Mizobuchi, Kei
Inooka, Taiga
Yoshitake, Kazutoshi
Minematsu, Naoko
Tsunoda, Kazushige
Kuniyoshi, Kazuki
Kawai, Yosuke
Omae, Yosuke
Tokunaga, Katsushi
Hayashi, Takaaki
Ueno, Shinji
Iwata, Takeshi
Appeared in: Genetics in medicine open
Paging: Volume 2 () nr. C pages p.
Year: 2024
Contents:
Publisher: The Authors
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 5 of 71 found articles
 
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