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  • Human IMPDH1 wild-type allele is located within 7q31.3-q32 and is approximately 18 kb in length. This allele, which encodes inosine-5\'-monophosphate dehydrogenase 1 protein, is involved in de novo synthesis of guanine nucleotides. Defects in the IMPDH1 gene cause autosomal dominant retinitis pigmentosa type 10.
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