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Case Report: A Novel Pathomechanism in PEComa by the Loss of Heterozygosity of TP53
Since the introduction of next-generation sequencing, the frequency of germline pathogenic TP53 variants and the number of cases with unusual clinical presentations have been increasing. This has led to the expansion of the classical Li–Fraumeni syndrome concept to a wider cancer predisposition synd...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995879/ https://www.ncbi.nlm.nih.gov/pubmed/35419288 http://dx.doi.org/10.3389/fonc.2022.849004 |