DGAT1 mutations leading to delayed chronic diarrhoea: a case report

BACKGROUND: Early-onset chronic diarrhoea often indicates a congenital disorder. Mutation in diacylglycerol o-acyltransferase 1 (DGAT1) has recently been linked to early-onset chronic diarrhoea. To date, only a few cases of DGAT1 deficiency have been reported. Diarrhoea in those cases was severe and...

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Detalles Bibliográficos
Autores principales: Xu, Luojia, Gu, Weizhong, Luo, Youyou, Lou, Jingan, Chen, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708908/
https://www.ncbi.nlm.nih.gov/pubmed/33261563
http://dx.doi.org/10.1186/s12881-020-01164-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708908/
https://www.ncbi.nlm.nih.gov/pubmed/33261563
http://dx.doi.org/10.1186/s12881-020-01164-1

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