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Table 1 Sequences of the primers used to validate the variant by Sanger sequencing

From: Neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies in a consanguineous Iranian family is associated with a homozygous start loss variant in the PRUNE1 gene

Gene Variant Primers
PRUNE1 NM_021222.3:c.3G>A
p.(Met1?)
Forward 5'ATTCGTCGGGGAAACCTCT 3'
Reverse 5'CTAAACTGGCTTCTCGCTCCT 3'