A founder nonsense variant in NUDT2 causes a recessive neurodevelopmental disorder in Saudi Arab children
H Yavuz1, A M Bertoli-Avella1, M Alfadhel2
1Centogene AG, Rostock, Germany.
Clinical Genetics
|July 31, 2018
Abstract:
We identified the homozygous p.Arg12* variant in 5 patients with neurodevelopmental delay, but variation databases list many truncating heterozygous variants for this small 2-exon gene. As most of these affect the protein's C-terminus, loss-of-function mediated pathogenicity may be confined to bi-allelic truncating variants in exon 1 (nonsense-mediated decay!) or in the catalytically active Nudix box.
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