Severe Combined Immunodeficiency (SCID) and Attention Deficit Hyperactivity Disorder (ADHD) Associated with a Coronin-1A Mutation and a Chromosome 16p11.2 Deletion

Defects causing severe combined immunodeficiency (SCID) have been reported in pathways mediating antigen receptor rearrangement, antigen receptor and cytokine signaling, and purine metabolism. Recognizing that the actin regulator Coronin-1A is essential for development of a normal peripheral T cell...

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Detaylı Bibliyografya
Asıl Yazarlar: Shiow, Lawrence R., Paris, Kenneth, Akana, Matthew C., Cyster, Jason G., Sorensen, Ricardo U., Puck, Jennifer M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2008
Konular:
Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2692687/
https://ncbi.nlm.nih.gov/pubmed/19097825
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.clim.2008.11.002
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