Publication | Closed Access
A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiency
11
Citations
13
References
2019
Year
Mitochondrial MyopathyMendelian DisorderGenetic DisorderGeneticsPathologyActa1 VariantMitochondrial ComplexMedicineNeuromusculoskeletal DisorderNemaline Myopathy
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