Whole-exome sequencing in a subject with fluctuating neuropsychiatric symptoms, immunoglobulin G1 deficiency, and subsequent development of Crohn’s disease: a case report

BACKGROUND: Mutations or polymorphisms of genes that are associated with inflammasome functions are known to predispose individuals to Crohn’s disease and likely affect clinical presentations and responses to therapeutic agents in patients with Crohn’s disease. The presence of additional gene mutati...

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Detalles Bibliográficos
Autores principales: Jyonouchi, Harumi, Geng, Lee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092677/
https://www.ncbi.nlm.nih.gov/pubmed/35538558
http://dx.doi.org/10.1186/s13256-022-03404-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9092677/
https://www.ncbi.nlm.nih.gov/pubmed/35538558
http://dx.doi.org/10.1186/s13256-022-03404-9

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