Clinical and genetic features of congenital dyserythropoietic anemia (CDA).

María-Isabel Moreno-CarraleroSaul Horta-HerreraMarta Morado-AriasMaría-Pilar Ricard-AndrésAngelina Lemes-CastellanoMariola Abio-CalveteMaría-Teresa Cedena-RomeroFernando-Ataulfo González-FernándezLaura Llorente-GonzálezAdela-María Periago-PeraltaSilvia de-la-Iglesia-ÍñigoManuel MéndezMaría-José Morán-Jiménez

Published in: European journal of haematology (2018)

New technologies for genetic studies will help to find variants in other genes, in addition to those known, that contribute to or modulate the CDA phenotype or support the correct diagnosis.

Keyphrases

genome wide
copy number
chronic kidney disease
dna methylation
gene expression
case control