A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis
Crossref DOI link: https://doi.org/10.1186/1546-0096-13-S1-O76
Published Online: 2015-09-28
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
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
Article History
First Online: 28 September 2015