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A novel homozygous exon 2 deletion of TRIM32 gene in patient with sarcotubular myopathy – case reportMarch 30, 2021 0Background Sarcotubular myopathy (STM) is a rare autosomal recessive disease characterized predominantly by weakness of the proximal limb. Mutations in the TRIM32 gene are often associated with STM and the limb-girdle muscular dystrophy R8 (LGMDR8). [...]
- March 11, 2021 0
- The development of antibiotics changed the world of medicine and has saved countless human and animal lives. Bacterial resistance/tolerance to antibiotics have spread silently across the world and has emerged as a major public health [...]