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SRRT Rabbit Polyclonal Antibody, 100ul Protein Expression Mutations in MTR have been

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SRRT Rabbit Polyclonal Antibody, 100ul Protein Expression Mutations in MTR have been

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Description

Mutations in MTR have been identified as the underlying cause of methylcobalamin deficiency complementation group G

This gene encodes a UDP-N-acetylglucosamine transporter found in the golgi apparatus membrane

MAP1LC3C is an ortholog of the yeast autophagosome protein Atg8 (He et al

It interacts with interferon regulatory factor-4 and plays an important role in immunoregulatory gene expression in B and T lymphocytes

A similar protein in mouse may be involved in regulating the effects of dopamine in the basal ganglia

SRRT Rabbit Polyclonal Antibody, 100ul Protein Expression Mutations in MTR have been

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