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

• Authors : Jian Zha; Ying Yu; Fangfang Cao

Subjects: brain structural abnormalities; congenital muscular dystrophy; epilepsy

• Source: Frontiers in Neurology, Vol 16 (2026)

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A Spectrum of Pathogenic Variants in the LAMA2 Gene in the Russian Federation

• Authors : Polina Chausova; Tatiana Cherevatova; Elena Dadali

Subjects: LAMA2 -associated muscular dystrophy; congenital muscular dystrophy; LAMA2 geneagris

• Source: International Journal of Molecular Sciences ; Volume 26 ; Issue 3 ; Pages: 1257

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A novel compound heterozygous variant in LAMA2 gene in a family with merosin-deficient congenital muscular dystrophy

• Authors : Parham Nejati; Nafiseh Falsafi; Elham Alimoradi

Subjects: LAMA2; Congenital muscular dystrophy; Whole-exome sequencing

• Source: BMC Medical Genomics, Vol 18, Iss 1, Pp 1-9 (2025)

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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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Primary dilated cardiomyopathy with LAMA2 and PKP4 mutations: imaging, genetics, and histology

• Authors : Zhou, Fang; Li, Jinghui; Lu, Minjie ...

• Source: European Heart Journal - Case Reports ; volume 10, issue 3 ; ISSN 2514-2119

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Early versus late diagnosis of LAMA2 congenital muscular dystrophy: a distinct consequence

• Authors : Chien-Heng Lin; Sheng-Shing Lin; Syuan-Yu Hong

Subjects: Early diagnosis; LAMA2 mutations; Muscular dystrophy

• Source: The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, Vol 60, Iss 1, Pp 1-5 (2024)

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The Interaction of LAMA2 and Duration of Illness Affects the Thickness of the Right Transverse Temporal Gyrus in Major Depressive Disorder

• Authors : Chen G; Li L; Sun T

Subjects: major depressive disorder; right transverse temporal gyrus; lama2

• Source: Neuropsychiatric Disease and Treatment, Vol Volume 19, Pp 2807-2816 (2023)

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

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

Subjects: case report; congenital muscular dystrophy type 1A; laminin subunit alpha 2 LAMA2

• Source: Frontiers in Genetics, Vol 14 (2023)

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

• Authors : Yuqing Xu; Linyan Zhu; Yeqing Qian

Subjects: LAMA2; LAMA2-related CMD; limb girdle muscular dystrophy 23

• Source: Frontiers in Pediatrics, Vol 11 (2023)

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

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

Subjects: merosin-deficient congenital muscular dystrophy type 1A; MDC1A; LAMA2 gene

• Source: Frontiers in Genetics, Vol 14 (2023)

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