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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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Foilsithe in: | Pediatr Rheumatol Online J |
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Main Authors: | , , , , , , , |
Formáid: | Artigo |
Teanga: | Inglês |
Foilsithe: |
BioMed Central
2016
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Ábhair: | |
Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5122026/ https://ncbi.nlm.nih.gov/pubmed/27881174 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12969-016-0124-2 |
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