Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo‐optico‐neuropathy (SMON)

Founder genetic variants of ABCC4 and ABCC11 in the Japanese population are not associated with the development of subacute myelo‐optico‐neuropathy (SMON)

Abstract Background Subacute myelo‐optico‐neuropathy (SMON) is a severe neurological disorder associated with clioquinol administration, which frequently occurred in Japan during the 1950s and 1960s. The unique genetic background of the Japanese population is considered to be strongly involved in th...

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Bibliographic Details
Main Authors: Hideki Matsumoto, Hideo Sasai, Norio Kawamoto, Masato Katsuyama, Makoto Minamiyama, Satoshi Kuru, Toshiyuki Fukao, Hidenori Ohnishi, SMON research group members
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Molecular Genetics & Genomic Medicine
Subjects:
ABCC11
ABCC4
clioquinol
Japanese
subacute myelo‐optico‐neuropathy
Online Access:https://doi.org/10.1002/mgg3.1845

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