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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...
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| Gepubliceerd in: | J Can Assoc Gastroenterol |
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| Hoofdauteurs: | , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2020
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7043697/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jcag/gwz047.105 |
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