Clinical and molecular analysis of patients with defects in μ heavy chain gene

Autosomal recessive disorders of B cell development are rare and heterogeneous. To determine the proportion of affected patients who have defects in the μ heavy chain (IGHM) gene, we used single-stranded conformational polymorphism analysis to screen genomic DNA from 40 unrelated patients with early...

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Autors principals: Lopez Granados, Eduardo, Porpiglia, Andrea S., Hogan, Mary Beth, Matamoros, Nuria, Krasovec, Silvia, Pignata, Claudio, Smith, C.I.E., Hammarstrom, Lennart, Bjorkander, Janne, Belohradsky, Bernd H., Casariego, G. Fontan, Garcia Rodriguez, M.C., Conley, Mary Ellen
Format: Artigo
Idioma:Inglês
Publicat: American Society for Clinical Investigation 2002
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC151150/
https://ncbi.nlm.nih.gov/pubmed/12370281
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI15658
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