A106 TTC7A MUTATION AND CHRONIC PRURITUS, A CASE REPORT

BACKGROUND: TTC7A mutation is a rare autosomal recessive disease that can present with various phenotypes including multiple intestinal atresia (MIA), very early onset inflammatory bowel disease (VEOIBD), and profound combined immunodeficiency with hypoplastic thymus, altered T- and B-cell maturatio...

Fuld beskrivelse

Na minha lista:
Bibliografiske detaljer
Udgivet i:J Can Assoc Gastroenterol
Main Authors: Hensen, M, Decaluwe, H, Haddad, E, Marchand, V
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2020
Fag:
Poster Presentation
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7043697/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwz047.105
Tags: Tilføj Tag
Ingen Tags, Vær først til at tagge denne postø!

Lignende værker