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Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are
Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are
Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are
Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are

Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are

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Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are

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Description

Mutations in this gene are associated with muscle glycogen storage disease

Mutations in TUBA1A cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

phospholipase A

This gene encodes a member of the semaphorin family of proteins

This protein associates with and regulated by other subunits of the complex including cyclin A or E

Human Mitochondrial Chaperone Bcs1, BCS1L ELISA Kit, 96T Microplate Mixer Mutations in this gene are

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