RET mutation p.S891A in a Chinese family with familial medullary thyroid carcinoma and associated cutaneous amyloidosis binding OSMR variant p.G513D

There are no reports on the relationship between familial medullary thyroid carcinoma (FMTC) associated with cutaneous amyloidosis (CA) and RET or OSMR/IL31RA gene mutations. In this study, we investigated a Chinese family with FMTC/CA and found a recurrent RET c.2671T>G (p.S891A) mutation in six...

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Detalhes bibliográficos
Publicado no:Oncotarget
Main Authors: Qi, Xiao-Ping, Zhao, Jian-Qiang, Chen, Zhen-Guang, Cao, Jin-Lin, Du, Juan, Liu, Nai-Fang, Li, Feng, Sheng, Mao, Fu, Er, Guo, Jian, Jia, Hong, Zhang, Yi-Ming, Ma, Ju-Ming
Formato: Artigo
Idioma:Inglês
Publicado em: Impact Journals LLC 2015
Assuntos:
Clinical Research Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4741820/
https://ncbi.nlm.nih.gov/pubmed/26356818
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