Determining oncogenic patterns and cancer predisposition through the transcriptomic profile in Mitchell–Riley syndrome with heterotopic gastric mucosa and duodenal atresia: a case report

BACKGROUND: Homozygous mutations in the transcription factor RFX6 are the cause of the Mitchell–Riley syndrome (MRS) associating neonatal diabetes, congenital digestive system, such as biliary atresia, pancreatic hypoplasia, duodenal and/or jejunal atresia, intestinal malrotation, gallbladder aplasi...

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Detalles Bibliográficos
Autores principales: Calcaterra, Valeria, Chiricosta, Luigi, Mazzon, Emanuela, Gugnandolo, Agnese, Alberti, Daniele, Maestri, Luciano, Meroni, Milena, Vestri, Elettra, Verduci, Elvira, Dilillo, Dario, Zuccotti, Gianvincenzo, Pelizzo, Gloria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556982/
https://www.ncbi.nlm.nih.gov/pubmed/34715892
http://dx.doi.org/10.1186/s13023-021-02093-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8556982/
https://www.ncbi.nlm.nih.gov/pubmed/34715892
http://dx.doi.org/10.1186/s13023-021-02093-9

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