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C15orf41 gene

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

Papers overview

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2020
2020
Background Congenital dyserythropoietic anaemia type I (CDA-I) is a hereditary anaemia caused by biallelic mutations in the… Expand
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2020
2020
Congenital dyserythropoietic anaemia (CDA) type I is a rare blood disorder characterised by moderate to severe macrocytic anaemia… Expand
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2020
2020
Background Congenital dyserythropoietic anemia type I (CDA I), is an autosomal recessive disease with macrocytic anemia in which… Expand
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2018
2018
Congenital dyserythropoietic anaemias (CDAs) are a group of rare haematological disorders characterized by ineffective… Expand
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2018
2018
INTRODUCTION Congenital dyserythropoietic anemias (CDA) are characterized by hyporegenerative anemia with inadequate reticulocyte… Expand
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2018
2018
Congenital dyserythropoietic anemias (CDAs) are rare hereditary blood disorders characterized by ineffective erythropoiesis… Expand
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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
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2016
2016
Hemolytic anemia with null PKLR mutations identified using whole exome sequencing and cured by hematopoietic stem cell… Expand
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Review
2013
Review
2013
The congenital dyserythropoietic anemias (CDAs) are hereditary disorders characterized by distinct morphologic abnormalities of… Expand
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2013
2013
The congenital dyserythropoietic anemias are a heterogeneous group of rare disorders primarily affecting erythropoiesis with… Expand
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