Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene

Podobne zapisy

• Diagnosis: Congenital Dyserythropoietic Anemia Type 2 Due to Compound Heterozygote Mutation in SEC23B Gene
  od: Fatih Demircioğlu, i wsp.
  Wydane: (2015-07-01)
• Congenital Dyserythropoietic Anemia Type II: molecular analysis and expression of the SEC23B Gene
  od: Punzo, Francesca, i wsp.
  Wydane: (2011)
• Maternal vitamin D supplementation and its impact on allergy
  od: Goksugur, Sevil Bilir, i wsp.
  Wydane: (2014)
• Hypomorphic mutations of SEC23B gene account for mild phenotypes of congenital dyserythropoietic anemia type II
  od: Russo, Roberta, i wsp.
  Wydane: (2013)
• Mutational spectrum in congenital dyserythropoietic anemia type II: Identification of 19 novel variants in SEC23B gene
  od: Russo, Roberta, i wsp.
  Wydane: (2010)