FA58A Polyclonal Antibody, 20ul Supplements HCFC1 is a member of
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FA58A Polyclonal Antibody, 20ul Supplements HCFC1 is a member ofMutations in this gene have been shown to cause an X linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin box fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
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