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Article

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

2015-01-01

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Literature Corpus work
e151cacb-0e72-55e3-8dc3-aeb8f99932c3
DOI
10.1186/1546-0096-13-s1-o76
PMCID
PMC4597329
Open publication

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A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritisDOI 10.1186/1546-0096-13-s1-o76
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