Trk A Polyclonal Antibody, 100ul[BT-AP09211] Glassware Sets Diseases associated with MYO1D include

Diseases associated with MYO1D include visceral heterotaxy

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Mutations at GCLC have been associated with hemolytic anemia due to deficiency of gamma-glutamylcysteine synthetase and susceptibility to myocardial infarction

Trk A Polyclonal Antibody, 100ul[BT-AP09211] Glassware Sets Diseases associated with MYO1D includeNTRK1 encodes a member of the neurotrophic tyrosine kinase receptor (NTKR) family. This kinase is a membrane bound receptor that, upon neurotrophin binding, phosphorylates itself and members of the MAPK pathway. The presence of this kinase leads to cell differentiation and may play a role in specifying sensory neuron subtypes. Mutations in this gene have been associated with congenital insensitivity to pain, anhidrosis, self mutilating behavior,