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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 : 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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Spanish Natural History Study for LAMA2 Muscular Dystrophy

• Authors : ASOCIACIÓN IMPÚLSATE PARA LA CURA DE LOS NIÑOS CON DÉFICIT DE MEROSINA

• Source: Spanish Natural History Study for LAMA2 Muscular Dystrophy

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

• Authors : Chausova, Polina¹ (AUTHOR) ; Cherevatova, Tatiana¹ (AUTHOR) ; Dadali, Elena¹ (AUTHOR)

• Source: International Journal of Molecular Sciences. Feb2025, Vol. 26 Issue 3, p1257. 14p.

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LAMA2 Genetic Correction

• Source: Ex Vivo Genetic Correction of LAMA2 Mutation(s) in Myogenic Stem Cells of Patients with Merosin-deficient Congenital Muscle Dystrophy Type 1a (MDC1a)

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Natural History Study of Children With LAMA2-related Dystrophies (LAMA2)

• Authors : Association Française contre les Myopathies (AFM), Paris

• Source: A Prospective, Longitudinal, Interventional Natural History Study of Children With LAMA2-related Dystrophies

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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 19, Pp 2807-2816 (2023)

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

• Authors : Lin, Chien-Heng^1,2 (AUTHOR); Lin, Sheng-Shing³ (AUTHOR); Hong, Syuan-Yu^3,4 (AUTHOR)

Subjects: *Muscular dystrophy; *Facioscapulohumeral muscular dystrophy; *Delayed diagnosis

• Source: Egyptian Journal of Neurology, Psychiatry & Neurosurgery. 1/5/2024, Vol. 60 Issue 1, p1-5. 5p.

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The Natural History of Patients With Mutations in SEPN1 (SELENON) or LAMA2

• Source: The Natural History of Patients With Congenital Muscular Dystrophies Due to Mutations in the SELENON or LAMA2 Genes: Working Towards Trial-readiness in Two Mitochondrial

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