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LAMA2 variants associated with muscular dystrophy, brain structural abnormalities, and epilepsy: a genotype-phenotype study

• Authors : Zha, Jian; Yu, Ying; Cao, Fangfang

• Source: Frontiers in Neurology ; volume 16 ; ISSN 1664-2295

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MYLK*FLNB and DOCK1*LAMA2 gene–gene interactions associated with rheumatoid arthritis in the focal adhesion pathway

• Authors : Veyssiere, Maëva; Rodriguez Ordonez, Maria del Pilar; Chalabi, Smahane

• Source: Frontiers in Genetics ; volume 15 ; ISSN 1664-8021

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Estimating the Prevalence of LAMA2 Congenital Muscular Dystrophy using Population Genetic Databases

• Authors : Lake, Nicole J.; Phua, Joel; Liu, Wei

• Source: Journal of Neuromuscular Diseases ; volume 10, issue 3, page 381-387 ; ISSN 2214-3599 2214-3602

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Merosin-deficient congenital muscular dystrophy type 1a: detection of LAMA2 variants in Vietnamese patients

• Authors : Tran, Van Khanh; Nguyen, Ngoc-Lan; Tran, Lan Ngoc Thi

• Source: Frontiers in Genetics ; volume 14 ; ISSN 1664-8021

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Identify and validate RUNX2 and LAMA2 as novel prognostic signatures and correlate with immune infiltrates in bladder cancer

• Authors : Jin, Yi; Huang, Siwei; Wang, Zhanwang

• Source: Frontiers in Oncology ; volume 13 ; ISSN 2234-943X

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Limb girdle muscular dystrophy 23 caused by compound heterozygous mutations of LAMA2 gene

• Authors : Xu, Yuqing; Zhu, Linyan; Qian, Yeqing ...

• Source: Frontiers in Pediatrics ; volume 11 ; ISSN 2296-2360

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Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous LAMA2 missense variant

• Authors : Katz, Matthew; Waddell, Leigh B.; Yuen, Michaela

• Source: Frontiers in Neurology ; volume 14 ; ISSN 1664-2295

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Case report: Novel frameshift mutation in LAMA2 gene causing congenital muscular dystrophy type 1A

• Authors : Diaz-Lombana, Natalia; Diaz-Ordoñez, Lorena; Gutierrez-Medina, Juan David

• Source: Frontiers in Genetics ; volume 14 ; ISSN 1664-8021

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Current Insights Into LAMA2 Disease

• Authors : Previtali, Stefano Carlo; Ruegg, Markus A; Cohn, Ronald

• Source: Frontiers Research Topics ; ISSN 1664-8714 ; ISBN 9782889740123

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Congenital muscular dystrophy in a dog with a LAMA2 gene deletion

• Authors : Shelton, G Diane; Minor, Katie M; Thomovsky, Stephanie

Subjects: 3009 Veterinary Sciences (for-2020); 30 Agricultural; Veterinary and Food Sciences (for-2020)279 - 284

• Source: Journal of Veterinary Internal Medicine, vol 36, iss 1

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