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Overview
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Calculated MW: 98 kDa
Observed MW: Refer to figures
Gene Accession: NP689846Please contact us at for specific academic pricing.
Background
This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus.
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