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NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

SKU: 54765343633

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NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

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Description

disease:Defects in MT-ND2 are a cause of Leber hereditary optic neuropathy (LHON)

The product of POLR2J exists as a heterodimer with another polymerase subunit

Hearing impairment is a heterogeneous condition with over 40 loci described

|Belongs to the Sp1 C2H2-type zinc-finger protein family

NO66 Rabbit Polyclonal Antibody, 20ul Recombinant Protein disease:Defects in MT-ND2 are a

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