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

Store: gaabil.dk · Domain: gaabil.dk

Description

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

The protein encoded by this gene belongs to the derlin family

[Isoform 2]: Only binds 2-AG with high affinity

The BimEL and BimL isoforms may be sequestered to the dynein motor complex through an interaction with the dynein light chain and released from this complex during apoptosis

IL8 and IL12B

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

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