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Germline Mutations for Novel Candidate Predisposition Genes in Sporadic Schwannomatosis
BACKGROUND: Schwannomatosis is a late-onset tumor predisposition syndrome associated with the development of many different types of malignancies. A relevant genetic mechanism can be explained by three mutational events. The first-hit mutation is a germline mutation, and the SMARCB1 mutation on chro...
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| Gepubliceerd in: | Clin Orthop Relat Res |
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| Hoofdauteurs: | , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Wolters Kluwer
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7571934/ https://ncbi.nlm.nih.gov/pubmed/32281771 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CORR.0000000000001239 |
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