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A Hereditary Form of Small Intestinal Carcinoid Associated with a Germline Mutation in Inositol Polyphosphate Multikinase

BACKGROUND & AIMS: Small intestinal carcinoids are rare and difficult to diagnose and patients often present with advanced, incurable disease. Although the disease occurs sporadically, there have been reports of family clusters. Hereditary small intestinal carcinoid has not been recognized and g...

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Detalhes bibliográficos
Publicado no:Gastroenterology
Main Authors: Sei, Yoshitatsu, Zhao, Xilin, Forbes, Joanne, Szymczak, Silke, Li, Qing, Trivedi, Apurva, Voellinger, Mark, Joy, Grishma, Feng, Jianying, Whatley, Millie, Jones, MaryPat Sussex, Harper, Ursula L., Marx, Stephen J., Venkatesan, Aradhana M., Chandrasekharappa, Settara C., Raffeld, Mark, Quezado, Martha M., Louie, Adeline, Chen, Clara C., Lim, Ramona M., Agarwala, Richa, Schäffer, Alejandro A., Hughes, Marybeth S., Bailey-Wilson, Joan E., Wank, Stephen A.
Formato: Artigo
Idioma:Inglês
Publicado em: 2015
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4858647/
https://ncbi.nlm.nih.gov/pubmed/25865046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1053/j.gastro.2015.04.008
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