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   A family carrying a homozygous LACC1 truncated mutation expands the clinical phenotype of this disease beyond systemic-onset juvenile idiopathic arthritis  
   
نویسنده arostegui j.i. ,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.
منبع pediatric rheumatology - 2015 - دوره : 13 - شماره : 1
چکیده    [no abstract available]
آدرس hospital clinic,immunology,barcelona, Spain, center for genomic regulation,barcelona, Spain, hospital la paz,pediatric rheumatology,madrid, Spain, hospital clinic,immunology,barcelona, Spain, hospital la paz,pediatric rheumatology,madrid, Spain, hospital la paz,pediatric rheumatology,madrid, Spain, hospital clinic,immunology,barcelona, Spain, center for genomic regulation,barcelona, Spain, hospital clinic,immunology,barcelona, Spain, center for genomic regulation,barcelona, Spain, universitat pompeu fabra,barcelona, Spain, center for genomic regulation,barcelona, Spain, hospital clinic,immunology,barcelona, Spain, center for genomic regulation,barcelona, Spain, hospital la paz,pediatric rheumatology,madrid, Spain
 
     
   
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