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Number of rare germline CNVs and TP53 mutation types
BACKGROUND: The Li-Fraumeni syndrome (LFS), an inherited rare cancer predisposition syndrome characterized by a variety of early-onset tumors, is caused by different highly penetrant germline mutations in the TP53 gene; each separate mutation has dissimilar functional and phenotypic effects, which p...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
BioMed Central
2012
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3558401/ https://ncbi.nlm.nih.gov/pubmed/23259501 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1750-1172-7-101 |
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