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Primary immunodeficiency diseases – genomic approaches delineate heterogeneous Mendelian disorders
BACKGROUND: Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous disorders thus far associated with mutations in more than 300 genes. The clinical phenotypes derived from distinct genotypes may overlap. Genetic etiology can be a prognostic indicator of disease sever...
Gespeichert in:
Veröffentlicht in: | J Allergy Clin Immunol |
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Hauptverfasser: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format: | Artigo |
Sprache: | Inglês |
Veröffentlicht: |
2016
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Schlagworte: | |
Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5222743/ https://ncbi.nlm.nih.gov/pubmed/27577878 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jaci.2016.05.042 |
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