Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations-Reference-Cited by-同舟云学术

Clinical and Pathological Heterogeneity of Korean Patients with CAPN3 Mutations

Published:2016 Issue:1 Volume:57 Page:173
ISSN:0513-5796
Container-title:Yonsei Medical Journal
language:en
Short-container-title:Yonsei Med J

Author:

Park Hyung Jun¹²,Jang Hoon³,Lee Jung Hwan²,Shin Ha Young²,Cho Sung-Rae¹,Park Kee Duk¹,Bang Duhee³,Lee Min Goo⁴,Kim Seung Min²,Lee Ji Hyun⁵,Choi Young-Chul²

Affiliation:

1. Department of Neurology, Mokdong Hospital, Ewha Womans University School of Medicine, Seoul, Korea.

2. Department of Neurology, Yonsei University College of Medicine, Seoul, Korea.

3. Department of Chemistry, Yonsei University, Seoul, Korea.

4. Department of Pharmacology, Pharmacogenomic Research Center for Membrane Transporters, Brain Korea 21 PLUS Project for Medical Sciences, Severance Biomedical Science Institute, Yonsei University College of Medicine, Seoul, Korea.

5. Department of Oral Biology, Yonsei University College of Dentistry, Seoul, Korea.

Funder

Korea Health Industry Development Institute

Publisher

Yonsei University College of Medicine

Subject

General Medicine

Link

http://synapse.koreamed.org/pdf/10.3349/ymj.2016.57.1.173

Cited by 9 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. Loss of Calpain 3 dysregulates store‐operated calcium entry and its exercise response in mice;The FASEB Journal;2024-07-19

2. Identification of novel pathogenic variants of Calpain-3 gene in limb girdle muscular dystrophy R1;Orphanet Journal of Rare Diseases;2024-04-01

3. Loss of calpain 3 dysregulates store-operated calcium entry and its exercise response in mice;2024-01-15

4. Single-centre experience with autosomal recessive limb-girdle muscular dystrophy: case series and literature review;Arquivos de Neuro-Psiquiatria;2023-10

5. Compound heterozygous CAPN3 variants identified in a family with limb-girdle muscular dystrophy recessive 1;Molecular Medicine Reports;2021-04-23