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MEF-2 (Acetyl Lys403) Rabbit Polyclonal Antibody, 100ul Primary Antibodies Mutation of this gene results

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MEF-2 (Acetyl Lys403) Rabbit Polyclonal Antibody, 100ul Primary Antibodies Mutation of this gene resultsdisease: Defects in MEF2A might be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

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Description

Mutation of this gene results in Brunner syndrome

Among its related pathways are Transport to the Golgi and subsequent modification and Surfactant metabolism

ACVR2A (activin A receptor type 2A) encodes a receptor that mediates the functions of activins

and the low density lipoprotein receptor (LDLR) family

MEF-2 (Acetyl Lys403) Rabbit Polyclonal Antibody, 100ul Primary Antibodies Mutation of this gene resultsdisease: Defects in MEF2A might be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

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