A Novel KCNA1 Mutation in an Episodic Ataxia Type 1 Patient with Asterixis and Falls

Ítems similars

• Clinical Spectrum of KCNA1 Mutations: New Insights into Episodic Ataxia and Epilepsy Comorbidity
  per: Paulhus, Kelsey, et al.
  Publicat: (2020)
• Dominant KCNA2 mutation causes episodic ataxia and pharmacoresponsive epilepsy
  per: Corbett, Mark A., et al.
  Publicat: (2016)
• A PATIENT WITH EPISODIC ATAXIA AND PARAMYOTONIA CONGENITA DUE TO MUTATIONS IN KCNA1 AND SCN4A
  per: Rajakulendran, S, et al.
  Publicat: (2009)
• Hypomorphic citrullinaemia due to mutated ASS1 with episodic ataxia
  per: Saini, Arushi Gahlot, et al.
  Publicat: (2018)
• Episodic Ataxia Type 2 due to a Deletion Mutation in the CACNA1A Gene in a Korean Family
  per: Kim, Jeong-Min, et al.
  Publicat: (2006)