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Identification of KRAS mutation in a patient with linear nevus sebaceous syndrome: a case report
BACKGROUND: Linear nevus sebaceous syndrome (LNSS) is a rare genetic disease characterized by large linear sebaceous nevus typically on the face, scalp, or neck. LNSS could be accompanied by multisystem disorders including the central nervous system. Herein, we report gene mutational profile via who...
| Autores principales: | , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2020
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7733249/ https://www.ncbi.nlm.nih.gov/pubmed/33308209 http://dx.doi.org/10.1186/s12920-020-00847-1 |