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S2546 Rabbit Polyclonal Antibody, 50ul In vitro Assessment Mutations in this gene have

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S2546 Rabbit Polyclonal Antibody, 50ul In vitro Assessment Mutations in this gene haveThis gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy.

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Description

Mutations in this gene have been associated with familial glucocorticoid deficiency type 2

CUL2 not CUL3

function:Polymorphonuclear leukocyte serine protease that degrades elastin

This protease is responsible for the degradation of aggrecan

S2546 Rabbit Polyclonal Antibody, 50ul In vitro Assessment Mutations in this gene haveThis gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy.

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