A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency.
In conclusion, we here describe a novel mutation in ADA, a well-known SCID gene.
PMID: 32245326 [PubMed - as supplied by publisher]
Source: Iranian Journal of Allergy, Asthma and Immunology - Category: Allergy & Immunology Authors: Talebi T, Biglari A, Shahroeei M, Changi-Ashtiani M, Dinmohammadi H, Navabi SS, Parvaneh N, Bossuyt X, Shahani T, Rokni-Zadeh H Tags: Iran J Allergy Asthma Immunol Source Type: research
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