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BioMed Central, Pediatric Rheumatology, S1(13), 2015

DOI: 10.1186/1546-0096-13-s1-o76

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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

Journal article published in 2015 by Ji Arostegui, R. Rabionet, A. Remesal, A. Mensa-Vilaro, S. Murias, R. Alcobendas, E. Gonzalez-Roca, O. Dreschsel, A. Puig, Estibaliz Ruiz-Ortiz ORCID, D. Comas, S. Ossowski ORCID, J. Yagüe ORCID, X. Estivill, R. Merino
This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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