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Mouse Pulmonary Surfactant-Associated Protein D, Sftpd ELISA Kit, 5*96T Glassware Mutations in SLC22A5 (solute carrier

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Mouse Pulmonary Surfactant-Associated Protein D, Sftpd ELISA Kit, 5*96T Glassware Mutations in SLC22A5 (solute carrier

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Description

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

Binds ganglioside Gt1b (PubMed: 8995428)

Members of this family share a common domain structure that consists of a transcription activation domain

and are clustered together on chromosome X

Five alternatively spliced transcripts encoding different proteins have been described

Mouse Pulmonary Surfactant-Associated Protein D, Sftpd ELISA Kit, 5*96T Glassware Mutations in SLC22A5 (solute carrier

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