Variant forms of X-linked severe combined immunodeficiency disease: one or many genes?

Immunodeficiency. 1993;4(1-4):253-8.

Authors

J P Disanto¹, F Le Deist, M Caniglia, S Markiewicz, Y Lebranchu, C Griscelli, A Fischer, G De Saint-Basile

Affiliation

¹ INSERM U 132, Hôpital Necker-Enfants Malades, Paris, France.

PMID: 8167713

No abstract available

MeSH terms

Child, Preschool
Chromosome Mapping
Dosage Compensation, Genetic
Female
Genetic Linkage
Genetic Variation
Heterozygote
Humans
Infant
Male
Mutation
Pedigree
Phenotype
Severe Combined Immunodeficiency / genetics*
Severe Combined Immunodeficiency / immunology
X Chromosome*