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Exome Sequencing Identifies a Novel SGCA Gene Mutation in an Iranian Family with Limb Girdle Muscular Dystrophy: A Case Report.
- Published in:
- Gene, Cell & Tissue, 2023, v. 10, n. 4, p. 1, doi. 10.5812/gct-135317
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- Article
Acute Renal Failure in a Patient with Coronavirus: A Case Report of a Rarely-Seen Presentation.
- Published in:
- Gene, Cell & Tissue, 2023, v. 10, n. 4, p. 1, doi. 10.5812/gct-135159
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- Article
Implications of Complement Imbalance in COVID-19: A Molecular Mechanistic Discussion on the Importance of Complement Balance.
- Published in:
- Iranian Journal of Immunology, 2023, v. 20, n. 3, p. 247, doi. 10.22034/iji.2023.97585.2522
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- Article
The homozygous pathogenic variant of the POMGNT1 gene identified using whole-exome sequencing in Iranian family with congenital hydrocephalus.
- Published in:
- Egyptian Journal of Medical Human Genetics, 2024, v. 25, n. 1, p. 1, doi. 10.1186/s43042-024-00513-6
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- Article