Nurit Batzir

Phenotypic expansion of POGZ-related intellectual disability syndrome (White-Sutton syndrome)

American Journal of Medical Genetics Part A · 2020 · First of 18 authors · 51 citations

Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy

Human Mutation · 2020 · First of 37 authors · 42 citations