Juvenile arthritis caused by a novel FAMIN (LACC1) mutation in two children with systemic and extended oligoarticular course

BACKGROUND: The pathophysiological origin of juvenile idiopathic arthritis (JIA) is largely unknown. However, individuals with presumably pathogenic mutations in FAMIN have been reported, associating this gene with a rare subtype of this disorder. FAMIN, that is formerly also referred to as LACC1 or...

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Detalles Bibliográficos
Autores principales: Kallinich, Tilmann, Thorwarth, Anne, von Stuckrad, Sae-Lim, Rösen-Wolff, Angela, Luksch, Hella, Hundsdoerfer, Patrick, Minden, Kirsten, Krawitz, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122026/
https://www.ncbi.nlm.nih.gov/pubmed/27881174
http://dx.doi.org/10.1186/s12969-016-0124-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5122026/
https://www.ncbi.nlm.nih.gov/pubmed/27881174
http://dx.doi.org/10.1186/s12969-016-0124-2

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