Novel DNMT3A Germline Variant in a Patient with Multiple Paragangliomas and Papillary Thyroid Carcinoma

SIMPLE SUMMARY: The use of next generation technologies has helped to unravel the genetics of rare inherited diseases, facilitating the discovery of new susceptibility genes. Nonetheless, the sequencing of all protein-coding genes of an individual may lead to doubtful assignments of causality for no...

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Detalles Bibliográficos
Autores principales: Mellid, Sara, Coloma, Javier, Calsina, Bruna, Monteagudo, María, Roldán-Romero, Juan M., Santos, María, Leandro-García, Luis J., Lanillos, Javier, Martínez-Montes, Ángel M., Rodríguez-Antona, Cristina, Montero-Conde, Cristina, Martínez-López, Joaquín, Ayala, Rosa, Matias-Guiu, Xavier, Robledo, Mercedes, Cascón, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697455/
https://www.ncbi.nlm.nih.gov/pubmed/33182397
http://dx.doi.org/10.3390/cancers12113304

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697455/
https://www.ncbi.nlm.nih.gov/pubmed/33182397
http://dx.doi.org/10.3390/cancers12113304

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