Metabolomics Distinguishes DOCK8 Deficiency from Atopic Dermatitis: Towards a Biomarker Discovery

Bi-allelic mutations in the dedicator of cytokinesis 8 (DOCK8) are responsible for a rare autosomal recessive primary combined immunodeficiency syndrome, characterized by atopic dermatitis, elevated serum Immunoglobulin E (IgE) levels, recurrent severe cutaneous viral infections, autoimmunity, and p...

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Detalles Bibliográficos
Autores principales: Jacob, Minnie, Gu, Xinyun, Luo, Xian, Al-Mousa, Hamoud, Arnaout, Rand, Al-Saud, Bandar, L. Lopata, Andreas, Li, Liang, Dasouki, Majed, Rahman, Anas M. Abdel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918408/
https://www.ncbi.nlm.nih.gov/pubmed/31718082
http://dx.doi.org/10.3390/metabo9110274

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6918408/
https://www.ncbi.nlm.nih.gov/pubmed/31718082
http://dx.doi.org/10.3390/metabo9110274

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