Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants

Roser Urreizti1,2, Jessica Vissicchio3, Mohamed Idries4

  • 1Clinical Biochemistry Department, Hospital Sant Joan de Déu. Institut de Recerca Sant Joan de Déu (IRSJD), Barcelona, Spain.

Summary

Genetic variants in TUBG1, crucial for cell division, can lead to neurological disorders. This study details two TUBG1 variants, linking them to conditions ranging from microcephaly and epilepsy to autism spectrum disorder.