Cargando…
The synergy of germline C634Y and V292M RET mutations in a northern Chinese family with multiple endocrine neoplasia type 2A
Genetic analysis for germline mutations of RET proto‐oncogene has provided a basis for individual management of medullary thyroid carcinoma (MTC) and pheochromocytoma. Most of compound mutations have more aggressive phenotypes than single point mutations, but the compound C634Y/V292M variant in MTC...
Autores principales: | Yang, Zheng, Qi, Xinmeng, Gross, Neil, Kou, Xiujuan, Bai, Yunlong, Feng, Yaru, Wang, Bochun, Zafereo, Mark E., Li, Guojun, Sun, Chuanzheng, Li, Huihui, Chen, Xiaohong, Huang, Zhigang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701567/ https://www.ncbi.nlm.nih.gov/pubmed/32989896 http://dx.doi.org/10.1111/jcmm.15922 |
Ejemplares similares
-
A large Chinese pedigree of multiple endocrine neoplasia type 2A with a novel C634Y/D707E germline mutation in RET exon 11
por: Lu, Fanqian, et al.
Publicado: (2017) -
Germline BRCA1 Mutation Detected in a Multiple Endocrine Neoplasia Type 2 Case With RET Codon 634 Mutation
por: Sarkadi, Balázs, et al.
Publicado: (2019) -
Long-term Clinicopathological Features of a Family with Multiple Endocrine Neoplasia Type 2A Caused by C634R RET Gene Mutation
por: Prabhu, Meghana, et al.
Publicado: (2020) -
Germline RET Leu56Met Variant Is Likely Not Causative of Multiple Endocrine Neoplasia Type 2
por: Hansen, Anna Reimer, et al.
Publicado: (2021) -
Late-Onset Medullary Thyroid Cancer in a Patient with a Germline RET Codon C634R Mutation
por: Walczyk, Agnieszka, et al.
Publicado: (2021)