Skip to search formSkip to main content
You are currently offline. Some features of the site may not work correctly.

C15orf41 gene

Known as: C15orf41, CHROMOSOME 15 OPEN READING FRAME 41, MGC11326 
National Institutes of Health

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Background Congenital dyserythropoietic anaemia type I (CDA-I) is a hereditary anaemia caused by biallelic mutations in the… Expand
2020
2020
Congenital dyserythropoietic anaemia (CDA) type I is a rare blood disorder characterised by moderate to severe macrocytic anaemia… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
2020
2020
Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which… Expand
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Review
2018
Review
2018
A 27-year-old African-American man presented with what was interpreted as non-immune haemolytic anaemia. He reported frequent… Expand
2018
2018
Congenital dyserythropoietic anaemias (CDAs) are a group of rare haematological disorders characterized by ineffective… Expand
2018
2018
Congenital dyserythropoietic anemias (CDA) are characterized by hyporegenerative anemia with inadequate reticulocyte values… Expand
2018
2018
Congenital dyserythropoietic anemias (CDAs) are rare hereditary blood disorders characterized by ineffective erythropoiesis… Expand
2016
2016
Hemolytic anemia with null PKLR mutations identified using whole exome sequencing and cured by hematopoietic stem cell… Expand
  • figure 1
  • figure 2
Review
2013
Review
2013
The congenital dyserythropoietic anemias (CDAs) are hereditary disorders characterized by distinct morphologic abnormalities of… Expand
  • table 1
  • figure 1
Highly Cited
2013
Highly Cited
2013
The congenital dyserythropoietic anemias are a heterogeneous group of rare disorders primarily affecting erythropoiesis with… Expand
  • figure 1
  • figure 2