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Cited by in F6Publishing
For: Bouman K, Gubbels M, van den Heuvel FM, Groothuis JT, Erasmus CE, Nijveldt R, Udink ten Cate FE, Voermans NC. Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy. Neuromuscular Disorders 2022. [DOI: 10.1016/j.nmd.2022.06.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
Number Citing Articles
1 Nouri Z, Sarmadi A, Narrei S, Sehhati M, Tabatabaiefar MA. Whole exome sequencing identified a novel LAMA2 frameshift variant causing merosin-deficient congenital muscular dystrophy in a patient with cardiomyopathy, and autism-like behaviors. Neuromuscular Disorders 2022. [DOI: 10.1016/j.nmd.2022.07.400] [Reference Citation Analysis]