Genotype-Phenotype Correlation ofSMN1andNAIPDeletions in Korean Patients with Spinal Muscular Atrophy-Reference-Cited by-同舟云学术

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Genotype-Phenotype Correlation ofSMN1andNAIPDeletions in Korean Patients with Spinal Muscular Atrophy

Published:2017 Issue:1 Volume:13 Page:27
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Ahn Eun-Ji¹,Yum Mi-Sun¹,Kim Eun-Hee²,Yoo Han-Wook¹³,Lee Beom Hee¹³,Kim Gu-Hwan³,Ko Tae-Sung¹

Affiliation:

1. Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

2. Department of Pediatrics, CHA Gangnam Medical Center, CHA University, Seoul, Korea.

3. Department of Medical Genetics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine, Seoul, Korea.

Publisher

Korean Neurological Association

Subject

Neurology (clinical),Neurology

Link

https://synapse.koreamed.org/pdf/10.3988/jcn.2017.13.1.27

Cited by 13 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Association among biomarkers, phenotypes, and motor milestones in Chinese patients with 5q spinal muscular atrophy types 1–3;Frontiers in Neurology;2024-09-02

2. Nusinersen Improves Motor Function in Type 2 and 3 Spinal Muscular Atrophy Patients across Time;Biomedicines;2024-08-06

3. Spinal muscular atrophy type I associated with a novel SMN1 splicing variant that disrupts the expression of the functional transcript;Frontiers in Neurology;2023-09-20

4. Emerging Gene Therapy Approaches in the Management of Spinal Muscular Atrophy (SMA): An Overview of Clinical Trials and Patent Landscape;International Journal of Molecular Sciences;2023-09-06

5. Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy;Journal of Clinical Medicine;2023-08-01

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