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A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis

Detalles Bibliográficos
Autores principales: Arostegui, JI, Rabionet, R, Remesal, A, Mensa-Vilaro, A, Murias, S, Alcobendas, R, Gonzalez-Roca, E, Dreschsel, O, Ruiz-Ortiz, E, Puig, A, Comas, D, Ossowski, S, Yagüe, J, Estivill, X, Merino, R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597329/
http://dx.doi.org/10.1186/1546-0096-13-S1-O76
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author Arostegui, JI
Rabionet, R
Remesal, A
Mensa-Vilaro, A
Murias, S
Alcobendas, R
Gonzalez-Roca, E
Dreschsel, O
Ruiz-Ortiz, E
Puig, A
Comas, D
Ossowski, S
Yagüe, J
Estivill, X
Merino, R
author_facet Arostegui, JI
Rabionet, R
Remesal, A
Mensa-Vilaro, A
Murias, S
Alcobendas, R
Gonzalez-Roca, E
Dreschsel, O
Ruiz-Ortiz, E
Puig, A
Comas, D
Ossowski, S
Yagüe, J
Estivill, X
Merino, R
author_sort Arostegui, JI
collection PubMed
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spelling pubmed-45973292015-10-08 A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis Arostegui, JI Rabionet, R Remesal, A Mensa-Vilaro, A Murias, S Alcobendas, R Gonzalez-Roca, E Dreschsel, O Ruiz-Ortiz, E Puig, A Comas, D Ossowski, S Yagüe, J Estivill, X Merino, R Pediatr Rheumatol Online J Oral Presentation BioMed Central 2015-09-28 /pmc/articles/PMC4597329/ http://dx.doi.org/10.1186/1546-0096-13-S1-O76 Text en Copyright © 2015 Arostegui et al. http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Oral Presentation
Arostegui, JI
Rabionet, R
Remesal, A
Mensa-Vilaro, A
Murias, S
Alcobendas, R
Gonzalez-Roca, E
Dreschsel, O
Ruiz-Ortiz, E
Puig, A
Comas, D
Ossowski, S
Yagüe, J
Estivill, X
Merino, R
A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title_full A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title_fullStr A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title_full_unstemmed A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title_short A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
title_sort family carrying a homozygous lacc1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
topic Oral Presentation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4597329/
http://dx.doi.org/10.1186/1546-0096-13-S1-O76
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