Mosaicism in X-linked severe combined immunodeficiency
- PMID: 9787703
- DOI: 10.1016/s0022-3476(98)70073-3
Mosaicism in X-linked severe combined immunodeficiency
Abstract
We performed gamma c gene analysis of a boy with severe combined immunodeficiency whose brother died of the same condition. A base pair deletion in exon 6 was found, which was absent in his mother, indicating maternal mosaicism with important implications for genetic counseling and demonstrating the importance of mutation analysis in boys with severe combined immunodeficiency.
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