Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study-Reference-Cited by-同舟云学术

Variants of aminoacyl‐tRNA synthetase genes in Charcot‐Marie‐Tooth disease: A Korean cohort study

Published:2021-12 Issue: Volume: Page:
ISSN:1085-9489
Container-title:Journal of the Peripheral Nervous System
language:en
Short-container-title:J Peripher Nerv Syst

Author:

Nam Da Eun¹,Park Jin Hee¹,Park Cho Eun¹,Jung Na Young¹,Nam Soo Hyun²,Kwon Hye Mi³,Kim Hyun Su⁴,Kim Sang Beom⁵^ORCID,Son Won Seok¹,Choi Byung‐Ok²³⁶,Chung Ki Wha¹^ORCID

Affiliation:

1. Department of Biological Sciences Kongju National University Gongju South Korea

2. Department of Health Sciences and Technology, SAIHST Sungkyunkwan University Seoul South Korea

3. Department of Neurology, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul South Korea

4. Department of Radiology, Samsung Medical Center Sungkyunkwan University School of Medicine Seoul South Korea

5. Department of Neurology Kyung Hee University Gangdong Hospital, Kyung Hee University College of Medicine Seoul South Korea

6. Stem Cell & Regenerative Medicine Institute Samsung Medical Center Seoul South Korea

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

Clinical Neurology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jns.12476

Reference39 articles.

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4. A major determinant for binding and aminoacylation of tRNA (Ala) in cytoplasmic Alanyl‐tRNA synthetase is mutated in dominant axonal Charcot‐Marie‐Tooth disease;Latour P;Am J Hum Genet,2010

5. Alanyl‐tRNA synthetase mutation in a family with dominant distal hereditary motor neuropathy;Zhao Z;Neurology,2012

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