Associated Papers
Two New Cases Expand the Phenotypic Spectrum of TUBG1 Missense Variants.
Urreizti R et al.
American Journal of Medical Genetics. Part A, 2025
Gamma-Tubulin 1 (TUBG1) Mutation-Associated Lissencephaly and Microcephaly in an Indian Child: A Rare Case.
Srivastava P et al.
Cureus, 2024
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