"Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis" by Bekim Sadikovic

Selected Works of Bekim Sadikovic

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Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis

Neuromuscular Disorders (2023)

Bekim Sadikovic, Western University

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Disciplines

Medicine and Health Sciences

Publication Date

2023

Citation Information

Bekim Sadikovic. "Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysis" Neuromuscular Disorders (2023)
Available at: http://works.bepress.com/bekim-sadikovic/28/