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S2546 Rabbit Polyclonal Antibody, 100ul Serum Mutations in this gene cause

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S2546 Rabbit Polyclonal Antibody, 100ul Serum Mutations in this gene causeThis 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 cause lissencephaly type 3 (LIS3) - a neurological condition characterized by microcephaly

developmental stage:Expressed in early stage of myeloid and erythroid differentiation

have been described for BRCA1

which may indicate an additional role in integrin signaling pathways

S2546 Rabbit Polyclonal Antibody, 100ul Serum Mutations in this gene causeThis 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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