Found: 4
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Spastic paraplegia 51: phenotypic spectrum related to novel homozygous AP4E1 mutation.
- Published in:
- Journal of Genetics, 2022, v. 101, n. 2, p. 1, doi. 10.1007/s12041-022-01385-8
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- Article
Targeting the MALAT1 gene with the CRISPR/Cas9 technique in prostate cancer.
- Published in:
- Genes & Environment, 2022, v. 44, n. 1, p. 1, doi. 10.1186/s41021-022-00252-3
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- Publication type:
- Article
Circulating Levels of Pro-inflammatory Cytokines in Patients with Nonalcoholic Fatty Liver Disease and Non-Alcoholic Steatohepatitis.
- Published in:
- Iranian Journal of Immunology, 2019, v. 16, n. 4, p. 327, doi. 10.22034/iji.2019.80284
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- Publication type:
- Article
Severe phenotype of an Iranian patient with methemoglobinemia type II due to a novel mutation in the CYB5R3 gene.
- Published in:
- Iranian Journal of Pediatric Hematology & Oncology, 2021, v. 11, n. 4, p. 280
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- Article