Structure of the Human Laminin α2-Chain Gene (LAMA2), Which Is Affected in Congenital Muscular Dystrophy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry
Reference45 articles.
1. Laminins and other strange proteins
2. The laminin family
3. The laminins
4. A new nomenclature for the laminins
5. Localization of the Gene (LAMA4) to Chromosome 6q21 and Isolation of a Partial cDNA Encoding a Variant Laminin A Chain
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1. Fatal Case of Exercise Collapse Associated with Sickle Cell Trait with Novel Underlying LAMA2 Mutation;American Journal of Forensic Medicine & Pathology;2024-01-23
2. Sleep in pediatric neuromuscular disorders;Seminars in Pediatric Neurology;2023-12
3. Estimating the Prevalence of LAMA2 Congenital Muscular Dystrophy using Population Genetic Databases;Journal of Neuromuscular Diseases;2023-05-02
4. LAMA2-Related Muscular Dystrophy: The Importance of Accurate Phenotyping and Brain Imaging in the Diagnosis of LGMD;Journal of Neuromuscular Diseases;2023-01-03
5. Estimating the prevalence of LAMA2 congenital muscular dystrophy using population genetic databases;2022-07-10
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