Muscle MRI findings in a one-year-old girl with merosin-deficient congenital muscular dystrophy type 1A due to LAMA2 mutation: A case report-Reference-Cited by-同舟云学术

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Muscle MRI findings in a one-year-old girl with merosin-deficient congenital muscular dystrophy type 1A due to LAMA2 mutation: A case report

Published:2017-06-29 Issue:2 Volume:7 Page:193-196
ISSN:2049-9434
Container-title:Biomedical Reports
language:en
Short-container-title:

Author:

Liang Yingyin,Li Guidian,Chen Songlin,He Rongxing,Zhou Xiangxue ,Chen Yingming,Xu Xue,Zhu Ronglan,Zhang Cheng

Publisher

Spandidos Publications

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Cited by 10 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. Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A;Frontiers in Genetics;2023-06-20

2. Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy;Neuromuscular Disorders;2022-08

3. Whole-body muscle MRI characteristics of LAMA2-related congenital muscular dystrophy children: An emerging pattern;Neuromuscular Disorders;2021-09

4. Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort;Orphanet Journal of Rare Diseases;2021-07-19

5. Exome Sequencing Reveals Diagnosis of LAMA2-Muscular Dystrophy and Possibility of Coexisting Bethlem Myopathy in a Neonate;Journal of Pediatric Neurology;2021-06-19

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