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SG1D4 Rabbit Polyclonal Antibody, 20ul Filtration Recently| patients with an unusual

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SG1D4 Rabbit Polyclonal Antibody, 20ul Filtration Recently| patients with an unusual

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Description

Recently| patients with an unusual autosomal-dominant bleeding disorder (factor V Quebec) were found to have a deficiency of platelet multimerin

nucleotide excision repair protein encoded by RAD23B is one of two human homologs of Saccharomyces cerevisiae Rad23

its exact function is not known

May play an important role in the pathogenesis of neurogenetic diseases

Alternative splicing of this gene generates two transcript variants diverging in the 3' region

SG1D4 Rabbit Polyclonal Antibody, 20ul Filtration Recently| patients with an unusual

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