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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
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, RVolume:
13
Year:
2015
Language:
english
Journal:
Pediatric Rheumatology
DOI:
10.1186/1546-0096-13-S1-O76
File:
PDF, 270 KB
english, 2015