Da E. Nam
Gongju, Republic of Korea
Last Updated: 09/26/2026
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Found 19 publications
Compound Heterozygous Mutations of SACS in a Korean Cohort Study of Charcot-Marie-Tooth Disease Concurrent Cerebellar Ataxia and Spasticity.
Journal: International journal of molecular sciences
Published: May 16, 2024
Gene Distribution in Pediatric-Onset Inherited Peripheral Neuropathy: A Single Tertiary Center in Thailand.
Journal: Journal of neuromuscular diseases
Published: November 06, 2023
Peripheral Neuropathy and Decreased Locomotion of a RAB40B Mutation in Human and Model Animals.
Journal: Experimental neurobiology
Published: August 30, 2023
Microsatellite Dataset for Cultivar Discrimination in Spring Orchid (Cymbidium goeringii).
Journal: Genes
Published: July 17, 2023
INF2 mutations in patients with a broad phenotypic spectrum of Charcot-Marie-Tooth disease and focal segmental glomerulosclerosis.
Journal: Journal of the peripheral nervous system : JPNS
Published: October 31, 2022
Peripheral Myelin Protein 22 Gene Mutations in Charcot-Marie-Tooth Disease Type 1E Patients.
Journal: Genes
Published: June 02, 2022
Variants of aminoacyl-tRNA synthetase genes in Charcot-Marie-Tooth disease: A Korean cohort study.
Journal: Journal of the peripheral nervous system : JPNS
Published: July 21, 2021
Clinical and Neuroimaging Features in Charcot-Marie-Tooth Patients with GNB4 Mutations.
Journal: Life (Basel, Switzerland)
Published: April 20, 2021
Homozygous mutations in Pakistani consanguineous families with prelingual nonsyndromic hearing loss.
Homozygous mutations in Pakistani consanguineous families with prelingual nonsyndromic hearing loss.
Journal: Molecular biology reports
Published: September 07, 2020
Paternal gender specificity and mild phenotypes in Charcot-Marie-Tooth type 1A patients with de novo 17p12 rearrangements.
Journal: Molecular genetics & genomic medicine
Published: November 08, 2019
Last Updated: 09/26/2026