HABP2 p.G534E variant in patients with family history of thyroid and breast cancer

Familial Papillary Thyroid Carcinoma (PTC) has been described as a hereditary predisposition cancer syndrome associated with mutations in candidate genes including HABP2. Two of 20 probands from families with history of PTC and breast carcinoma (BC) were evaluated by whole exome sequencing (WES) rev...

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Detalles Bibliográficos
Autores principales: Pinheiro, Maisa, Drigo, Sandra Aparecida, Tonhosolo, Renata, Andrade, Sonia C.S., Marchi, Fabio Albuquerque, Jurisica, Igor, Kowalski, Luiz Paulo, Achatz, Maria Isabel, Rogatto, Silvia Regina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522276/
https://www.ncbi.nlm.nih.gov/pubmed/28402931
http://dx.doi.org/10.18632/oncotarget.16639

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522276/
https://www.ncbi.nlm.nih.gov/pubmed/28402931
http://dx.doi.org/10.18632/oncotarget.16639

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