Your search for "dym" returned 731 TaqMan® SNP Genotyping Assays
This gene encodes a protein which is necessary for normal skeletal development and brain function. Mutations in this gene are associated with two types of recessive osteochondrodysplasia, Dyggve-Melchior-Clausen (DMC) dysplasia and Smith-McCort (SMC) dysplasia, which involve both skeletal defects and mental retardation. [provided by RefSeq, Jul 2008]
1810041M12RIK, 4933427L07RIK, C030019K18RIK, DMC, DYM, RGD1309111, SMC
Please enter the information below and press OK to send your cart to Core Services for purchase.