DYM: Difference between revisions
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| summary_text = 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.<ref name="entrez" |
| summary_text = 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.<ref name="entrez"/> |
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Revision as of 05:02, 17 June 2009
Template:PBB Dymeclin, also known as DYM, is a human gene.[1]
References
Further reading
 | This article on a gene on human chromosome 18 is a stub. You can help Wikipedia by expanding it. |