DYM
Template:Short description Script error: No such module "redirect hatnote". Template:Infobox gene Dymeclin is a protein that in humans is encoded by the DYM gene.[1]
This gene encodes a protein which is necessary for normal skeletal development and brain function and has been first described and named in 2003.[2] Mutations in this gene are associated with two types of recessive osteochondrodysplasias, Dyggve-Melchior-Clausen (DMC) syndrome, which involves both skeletal defects and postnatal microcephaly with intellectual deficiency, and Smith-McCort (SMC) dysplasia, which involves skeletal defects only.[1]
References
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Further reading
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