A novel mutation in SLC37A4 gene in a Sri Lankan boy with glycogen storage disease type Ib associated with very early onset neutropenia

Lignende værker

• A Sri Lankan child with 49,XXXXY syndrome
  af: Dissanayake, Vajira H. W., et al.
  Udgivet: (2010)
• Clinical and genetic features of Huntington disease in Sri Lanka
  af: Sumathipala, Dulika S, et al.
  Udgivet: (2013)
• A Case Series of Five Sri Lankan Patients with Ovotesticular Disorder of Sex Development
  af: Wettasinghe, Kalum T., et al.
  Udgivet: (2012)
• Autosomal dominant hereditary ataxia in Sri Lanka
  af: Sumathipala, Dulika S, et al.
  Udgivet: (2013)
• Novel SLC37A4 Mutations in Korean Patients With Glycogen Storage Disease Ib
  af: Choi, Rihwa, et al.
  Udgivet: (2017)