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...

Descrición completa

Gardado en:
Detalles 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: American Society for Clinical Investigation 2002
Assuntos:
Article
Acceso en liña: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
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares