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PALM3 Rabbit Polyclonal Antibody, 20ul Proteases Mutations in this gene cause

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PALM3 Rabbit Polyclonal Antibody, 20ul Proteases Mutations in this gene cause

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Description

Mutations in this gene cause spastic paraplegia autosomal dominant type 31

The encoded protein is a class 3 semaphorin receptor| and may be involved in cytoskeletal remodeling and as well as apoptosis

Mutations in this gene have be associated with autosomal recessive Segawa syndrome

Studies suggest that the N-terminal region of this protein interacts with Atxn1 (GeneID:6310)

PALM3 Rabbit Polyclonal Antibody, 20ul Proteases Mutations in this gene cause

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