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Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype

Detalles Bibliográficos
Autores principales: Santos, J, Arostégui, JI, Brito, MJ, Neves, C, Conde, M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194569/
http://dx.doi.org/10.1186/1546-0096-9-S1-P21
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author Santos, J
Arostégui, JI
Brito, MJ
Neves, C
Conde, M
author_facet Santos, J
Arostégui, JI
Brito, MJ
Neves, C
Conde, M
author_sort Santos, J
collection PubMed
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spelling pubmed-31945692011-10-18 Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype Santos, J Arostégui, JI Brito, MJ Neves, C Conde, M Pediatr Rheumatol Online J Poster Presentation BioMed Central 2011-09-14 /pmc/articles/PMC3194569/ http://dx.doi.org/10.1186/1546-0096-9-S1-P21 Text en Copyright ©2011 Santos et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Poster Presentation
Santos, J
Arostégui, JI
Brito, MJ
Neves, C
Conde, M
Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title_full Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title_fullStr Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title_full_unstemmed Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title_short Hyper-IgD syndrome: a new mutation (p.R277G) with a severe phenotype
title_sort hyper-igd syndrome: a new mutation (p.r277g) with a severe phenotype
topic Poster Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194569/
http://dx.doi.org/10.1186/1546-0096-9-S1-P21
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