Dymeclin 抗体
(Dymeclin (DYM))
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].
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Aliases for Dymeclin 抗体
dymeclin (DYM) 抗体dymeclin (dym) 抗体
dymeclin (Dym) 抗体
dymeclin L homeolog (dym.L) 抗体
1810041M12Rik 抗体
4933427L07Rik 抗体
C030019K18Rik 抗体
DMC 抗体
DYM 抗体
dym 抗体
LOC734107 抗体
RGD1309111 抗体
SMC 抗体
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