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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.

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Description scientific article
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author: Anna Puig  Anna Mensa-Vilaro  Eva Gonzalez-Roca  Xavier Estivill i Pallejà  David Comas  Stephan Ossowski  Raquel Rabionet  Juan I Arostegui  Estibaliz Ruiz-Ortiz 

Publication date September 28, 2015
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