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KRA54 Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification disease:Defects in MT-ND2 are a

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KRA54 Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification 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)

which is involved in the etiology of autism and eventually increases autism risk through interaction with another subunit

Alternative splici

including regulating neurotransmitter and hormone release

members of which coat intracellular lipid storage droplets

KRA54 Rabbit Polyclonal Antibody, 20ul Protein Post-translational Modification disease:Defects in MT-ND2 are a

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