Juvenile Idiopathic Arthritis exome sequencing in a consanguineous family

Identify the causative gene defect in three affected patients with JIA.

1 Dataset 1 Publication

Click on a Dataset ID in the table below to learn more, and to find out who to contact about access to these data

Dataset ID	Description	Technology	Samples
EGAD00001004806	Exome sequencing data for two sibs with juvenile idiopathic arthitis and one unaffected sib	Illumina Genome Analyzer II	3

Publications	Citations
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis. Rabionet R, Remesal A, Mensa-Vilaró A, Murías S, Alcobendas R, González-Roca E, Ruiz-Ortiz E, Antón J, Iglesias E, Modesto C, Comas D, Puig A, Drechsel O, Ossowski S, Yagüe J, Merino R, Estivill X, Arostegui JI. Sci Rep 9: 2019 4579	12