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ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifested
ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifested
ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifested
ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifested

ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifested

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ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifestedThis gene encodes a protein containing an alpha beta hydrolase fold which is a catalytic domain found in a very wide range of enzymes. The function of this protein has not been determined.

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Description

an autosomal recessive disorder manifested early in life by hypoketotic hypoglycemia and acute metabolic decompensation

TLR9 and TRAF6

The sealing cap can be opened and closed repeatedly

This gene is thought to be involved in CNS development

Pseudogenes of this gene are found on chromosomes 13 and 17

ABHD3 Polyclonal Antibody, 50ul Molecular Biologyn an autosomal recessive disorder manifestedThis gene encodes a protein containing an alpha beta hydrolase fold which is a catalytic domain found in a very wide range of enzymes. The function of this protein has not been determined.

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