Your search for "tspear" returned 881 TaqMan® SNP Genotyping Assays
thrombospondin type laminin G domain and EAR repeats
This gene encodes a protein that contains a N-terminal thrombospondin-type laminin G domain and several tandem arranged epilepsy-associated repeats (EARs). A mutation in this gene is the cause of autosomal recessive deafness-98. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Dec 2012]
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