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UN13D Rabbit Polyclonal Antibody, 100ul Vector Construction Mutations in this gene cause

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UN13D Rabbit Polyclonal Antibody, 100ul Vector Construction Mutations in this gene cause

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Description

Mutations in this gene cause primary ciliary dyskinesia type 3| as well as Kartagener syndrome| which are both diseases due to ciliary defects

Read-through transcription also exists between this gene and the downstream chromosome 6 open reading frame 26 (C6orf26) gene

including hunger

and can also affect the permeability of blood vessels

UN13D Rabbit Polyclonal Antibody, 100ul Vector Construction Mutations in this gene cause

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