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Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are
Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are
Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are
Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are

Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are

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Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are

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Description

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

The encoded adhesion protein is found in cochlear outer hair cells and appears to be important for proper hearing over an extended frequency range

Active against a broad range of microbes

The precursor seems to be activated while it is being transported along the axon to the posterior pituitary

Has lower chemotactic activity for neutrophils but none for monocytes and activated lymphocytes

Human Aldehyde Dehydrogenase Family 1 Member A3, ALDH1A3 ELISA Kit, 96T sgRNA Library Construction Mutations in this gene are

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