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Two novel ADAR1 gene mutations in two patients with dyschromatosis symmetrical hereditaria from birth.
- Published in:
- Molecular Medicine Reports, 2017, v. 15, n. 6, p. 3715, doi. 10.3892/mmr.2017.6427
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Single-cell transcriptomic analysis reveals the critical molecular pattern of UV-induced cutaneous squamous cell carcinoma.
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- Cell Death & Disease, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41419-021-04477-y
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- Publication type:
- Article
Novel mutations in one allele in a Chinese family with neurofibromatosis type 1: Including a complex insertion-deletion mutation.
- Published in:
- Journal of Dermatology, 2016, v. 43, n. 11, p. 1332, doi. 10.1111/1346-8138.13498
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- Article