Compound heterozygous CAPN3 variants identified in a family with limb-girdle muscular dystrophy recessive 1-Reference-Cited by-同舟云学术

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Compound heterozygous CAPN3 variants identified in a family with limb-girdle muscular dystrophy recessive 1

Published:2021-04-23 Issue:6 Volume:23 Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Rep

Author:

Zhang Cheng¹,Zheng Xueping²,Lu Deguo³,Xu Lulu²,Che Fengyuan³,Liu Shiguo¹

Affiliation:

1. Medical Genetic Department, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China

2. Department of Geriatric Medicine, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China

3. Department of Neurology, The Eleventh Clinical Medical College of Qingdao University, Linyi People's Hospital, Linyi, Shandong 276000, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 2 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. In-situ inhibition mechanism of SO3 formation over MoS2 modified V2O5/TiO2 catalyst within selective catalytic reduction process;Fuel;2024-11

2. Missense mutation of c.635 T > C in CAPN3 impairs muscle injury repair in a Limb‐Girdel Muscular Dystropy Model;Clinical Genetics;2023-03-31

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