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    • Fetal medicine and pathology (WG6)
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    • Guidelines & consensus (WG11)
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    • ERN ITHACA Guidelines
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    • Documentation for patients
  • News & Events
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Home > Our Research Activities > List Of Publications > TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations

TUBB3 E410K syndrome: Case report and review of the clinical spectrum of TUBB3 mutations

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TUBB Variants Underlying Different Phenotypes Result in Altered Vesicle Trafficking and Microtubule Dynamics
Very mild isolated intellectual disability caused by adenylosuccinate lyase deficiency: a new phenotype
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