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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Clinical Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741820/
https://www.ncbi.nlm.nih.gov/pubmed/26356818

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