Rare variants inmethionyl- andtyrosyl-tRNA synthetasegenes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy-Reference-Cited by-同舟云学术

Rare variants inmethionyl- andtyrosyl-tRNA synthetasegenes in late-onset autosomal dominant Charcot-Marie-Tooth neuropathy

Author:

Hyun Y.S.¹,Park H.J.²,Heo S.-H.³,Yoon B.R.¹,Nam S.H.¹,Kim S.-B.⁴,Park C.I.⁵,Choi B.-O.²,Chung K.W.¹

Affiliation:

1. Department of Biological Science; Kongju National University; Gongju Korea

2. Department of Neurology, Samsung Medical Center; Sungkyunkwan University School of Medicine; Seoul Korea

3. The National Project for Rehabilitative Robot Translational Research; Ministry of Health and Welfare; Cheongwon-gun Korea

4. Department of Neurology; Kyung Hee University College of Medicine, Kangdong Hospital; Seoul Korea

5. Department of Neurology; Yonsei University Wonju College of Medicine; Wonju Korea

Funder

Ministry of Health & Welfare in Republic of Korea

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference7 articles.

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