Condition: Keratoconjunctivitis Sicca


rs151344517 in LOC107985154;AFG3L2;TUBB6 gene and Keratoconjunctivitis Sicca PMID 20725928 2010 Missense mutations in the AFG3L2 proteolytic domain account for ∼1.5% of European autosomal dominant cerebellar ataxias.