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NDRG3

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For Research Use Only. Not For Clinical Use.


NDRG3 (NDRG Family Member 3) is a Protein Coding gene. Diseases associated with NDRG3 include Charcot-Marie-Tooth Disease, Type 4D and Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive. Among its related pathways are PI3K / Akt Signaling and Apoptosis and Autophagy. An important paralog of this gene is NDRG1.
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