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

J. I. Arostegui, R. Rabionet, A. Remesal, A. Mensa-Vilaro, S. Murias, R. Alcobendas, E. Gonzalez-Roca, O. Dreschsel, E. Ruiz-Ortiz, A. Puig, D. Comas, S. Ossowski, J. Yagüe, Xavier P. Estivill, R. Merino

Research output: Contribution to journalArticle

6 Citations (Scopus)
Original languageEnglish
Article numberO76
JournalPediatric Rheumatology
Volume13
Issue number1
DOIs
Publication statusPublished - 28 Sep 2015
Externally publishedYes

ASJC Scopus subject areas

  • Rheumatology
  • Immunology and Allergy
  • Pediatrics, Perinatology, and Child Health

Cite this