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SPDE7 Rabbit Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in this gene cause

SKU: 63922474121

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SPDE7 Rabbit Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in this gene cause

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Description

Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II

contains a GTP-binding motif

In addition| it has been shown to be significantly overexpressed in several human tumors

Belongs to the protein kinase superfamily

Mutations and deletions in NKX2-1 are associated with benign hereditary chorea

SPDE7 Rabbit Polyclonal Antibody, 50ul Reagent Reservoirs Mutations in this gene cause

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