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

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

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

ISSN: 1755-8794