A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency.

Talebi, Taravat

A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency. [electronic resource] - Iranian journal of allergy, asthma, and immunology Feb 2020 - 94-101 p. digital

Publication Type: Case Reports; Journal Article

1735-5249

10.18502/ijaai.v19i1.2422 doi


Adenosine Deaminase--deficiency
Agammaglobulinemia--genetics
Female
Humans
Infant
Iran
Male
Mutation
Pedigree
Severe Combined Immunodeficiency--genetics
Exome Sequencing