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YT011 Rabbit Polyclonal Antibody, 100ul Oligo Pool Mutations in PNPT1 have been

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YT011 Rabbit Polyclonal Antibody, 100ul Oligo Pool Mutations in PNPT1 have been

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Description

Mutations in PNPT1 have been associated with combined oxidative phosphorylation deficiency-13 and autosomal recessive nonsyndromic deafness-70

but particularly in cells of the immune and nervous systems

The specific functions of these proteins have not been determined| but they are thought to be involved in sperm maturation

Defects in this gene have also been associated with non-familial structural atrial fibrillation

YT011 Rabbit Polyclonal Antibody, 100ul Oligo Pool Mutations in PNPT1 have been

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