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PMID: 11410213 Published · ppublish English Journal Article Review

Primary immunodeficiency diseases: an experimental model for molecular medicine.

Lancet (London, England) ·Vol. 357 ·No. 9271 ·2001-06-09 ·Pages 1863-9

Fischer A

Abstract

Primary immunodeficiency diseases represent a vast array of inherited disorders of the immune system. Major advances in the understanding of genetic basis and molecular mechanisms have occurred within the past 10 years, as a result of the tools of modern genetics. About three quarters of 100 primary immunodeficiency diseases can now be reliably diagnosed with molecular probes. In many cases, gene identification has enabled significant insight into the physiopathology of the related conditions. Therapeutic progress based on protein engineering and possibly gene therapy will also ensue.

MeSH Terms
Genetic Therapy Humans Immunologic Deficiency Syndromes/diagnosis,genetics,therapy Molecular Probes Phenotype Protein Engineering
Chemicals
Molecular Probes
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Fischer A
INSERM U429, Hôpital Necker, 149 Rue de Sévres, 75015, Paris, France. fischer@necker.fr
Article Info
Journal
Lancet (London, England)
Abbr.
Lancet
ISSN
0140-6736
Published
2001-06-09
Pages
1863-9
Language
English
Region
England
NLM ID
2985213R
Subset
IM
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