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
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