Increased frequency of homozygosity of abnormal mannan-binding-protein alleles in patients with suspected immunodeficiency
- 1 October 1995
- journal article
- research article
- Published by Elsevier BV in The Lancet
- Vol. 346 (8980), 941-943
- https://doi.org/10.1016/s0140-6736(95)91559-1
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Mannose binding protein gene mutations associated with unusual and severe infections in adultsThe Lancet, 1995
- DUAL ROLE OF MANNAN‐BINDING PROTEIN IN INFECTIONS: ANOTHER CASE OF HETEROSIS?International Journal of Immunogenetics, 1994
- A new frequent allele is the missing link in the structural polymorphism of the human mannan-binding proteinImmunogenetics, 1994
- Mannan-binding protein—levels in plasma and upper-airways secretions and frequency of genotypes in children with recurrence of otitis mediaClinical and Experimental Immunology, 1993
- DIALLELIC POLYMORPHISM MAY EXPLAIN VARIATIONS OF THE BLOOD CONCENTRATION OF MANNAN‐BINDING PROTEIN IN ESKIMOS, BUT NOT IN BLACK AFRICANSInternational Journal of Immunogenetics, 1992
- High frequencies in African and non-African populations of independent mutations in the mannose binding protein geneHuman Molecular Genetics, 1992
- Gene frequency and partial protein characterization of an allelic variant of mannan binding protein associated with low serum concentrationsClinical and Experimental Immunology, 1992
- Molecular basis of opsonic defect in immunodeficient childrenThe Lancet, 1991