Found: 4
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Late-onset hereditary sensory and autonomic neuropathy type 2B caused by novel compound heterozygous mutations in FAM134B presenting as chronic recurrent ulcers on the soles.
- Published in:
- 2021
- By:
- Publication type:
- case study
Novel mutations in associated with dyschromatosis universalis hereditaria.
- Published in:
- 2019
- By:
- Publication type:
- letter
Neonatal hereditary dystrophic epidermolysis bullosa: a genetically diagnosed case report.
- Published in:
- Journal of Health Sciences of Peking University / Beijing Daxue Xuebao (Yixue Ban), 2013, v. 45, n. 2, p. 202, doi. 10.3969/j.issn.1671-167X.2013.02.008
- By:
- Publication type:
- Article
Preparation of a liposomal delivery system and its in vitro release of rapamycin.
- Published in:
- Experimental & Therapeutic Medicine, 2015, v. 9, n. 3, p. 941, doi. 10.3892/etm.2015.2201
- By:
- Publication type:
- Article