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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Detalhes bibliográficos
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: American Society for Clinical Investigation 2002
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Article
Acesso em linha: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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