Dysarthria, Ataxia, and Dystonia Associated with COX20 (FAM36A) Gene Mutation: A Case Report of a Turkish Child

Lignende værker

• Spinocerebellar Ataxia-21 in a Turkish Child
  af: Incecik, Faruk, et al.
  Udgivet: (2018)
• Clinical Features and Molecular Genetics of Autosomal Recessive Ataxia in the Turkish Population
  af: Incecik, Faruk, et al.
  Udgivet: (2020)
• Late-Onset Leigh Syndrome due to NDUFV1 Mutation in a 10-Year-Old Boy Initially Presenting with Ataxia
  af: Incecik, Faruk, et al.
  Udgivet: (2018)
• Autosomal-Recessive Spastic Ataxia of Charlevoix-Saguenay: A Turkish Child
  af: Incecik, Faruk, et al.
  Udgivet: (2018)
• D-bifunctional Protein Deficiency: A Case Report of a Turkish Child
  af: Incecik, Faruk, et al.
  Udgivet: (2019)