Corrigendum to “First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children” [Mol. Genet. Metab. Rep. 2 (2016) 81–84]

Lignende værker

• First contiguous gene deletion causing biotinidase deficiency: The enzyme deficiency in three Sri Lankan children
  af: Senanayake, Danika Nadeen, et al.
  Udgivet: (2015)
• Developmental window of sensorineural deafness in biotinidase-deficient mice
  af: Maheras, Kathleen June, et al.
  Udgivet: (2017)
• Cornea Verticillata in classical Fabry disease, first from Sri Lanka: a case report
  af: Hewavitharana, Hasani, et al.
  Udgivet: (2020)
• Differential gene expression during early development in brains of wildtype and biotinidase-deficient mice
  af: Brigolin, Christian, et al.
  Udgivet: (2016)
• Neurological deficits in mice with profound biotinidase deficiency are associated with demylination and axonal degeneration
  af: Pindolia, Kirit, et al.
  Udgivet: (2012)