Atypical X-linked severe combined immunodeficiency due to possible spontaneous reversion of the genetic defect in T cells

N Engl J Med. 1996 Nov 21;335(21):1563-7. doi: 10.1056/NEJM199611213352104.

Authors

V Stephan¹, V Wahn, F Le Deist, U Dirksen, B Broker, I Müller-Fleckenstein, G Horneff, H Schroten, A Fischer, G de Saint Basile

Affiliation

¹ Universitätskinderklinik, Heinrich-Heine Universität, Düsseldorf, Germany.

PMID: 8900089
DOI: 10.1056/NEJM199611213352104

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

B-Lymphocytes / immunology
Base Sequence
Genetic Linkage
Humans
Infant
Lymphocyte Count
Male
Point Mutation
Receptors, Interleukin-2 / genetics*
Severe Combined Immunodeficiency / genetics*
Severe Combined Immunodeficiency / immunology
T-Lymphocytes / immunology*
X Chromosome

Substances

Receptors, Interleukin-2