The RET C611Y mutation causes MEN 2A and associated cutaneous lichen amyloidosis

BACKGROUND: Cutaneous lichen amyloidosis (CLA) has been reported in some multiple endocrine neoplasia type 2A (MEN 2A) families affected by specific germline RET mutations C634F/G/R/W/Y or V804M, as a characteristic of the clinical manifestation in ‘MEN 2A with CLA’, one of four variants of MEN 2A,...

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Detalhes bibliográficos
Publicado no:Endocr Connect
Main Authors: Qi, Xiao-Ping, Peng, Jian-Zhong, Yang, Xiao-Wei, Cao, Zhi-Lie, Yu, Xiu-Hua, Fang, Xu-Dong, Zhang, Da-Hong, Zhao, Jian-Qiang
Formato: Artigo
Idioma:Inglês
Publicado em: Bioscientifica Ltd 2018
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Research
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6176283/
https://ncbi.nlm.nih.gov/pubmed/30300539
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1530/EC-18-0220
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