Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III-Reference-Cited by-同舟云学术

Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III

Published:2022-10-06 Issue:2 Volume:108 Page:581-587
ISSN:1592-8721
Container-title:Haematologica
language:
Short-container-title:haematol

Author:

Hernández Gonzalo,Romero-Cortadellas Lídia,Ferrer-Cortès Xènia,Venturi Veronica,Dessy-Rodriguez Mercedes,Olivella Mireia,Husami Ammar,De Soto Concepción Pérez,Morales-Camacho Rosario M.,Villegas Ana,González-Fernández Fernando-Ataulfo,Morado Marta,Kalfa Theodosia A.,Quintana-Bustamante Oscar,Pérez-Montero Santiago,Tornador Cristian,Segovia Jose-Carlos,Sánchez Mayka

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Reference15 articles.

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2. Méndez M, Moreno-Carralero MI, Peri VL. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene. Ann Hematol. 2021; 100(2):353-364.

3. Pavicic-Kaltenbrunner V, Mishima M, Glotzer M. Cooperative assembly of CYK-4/MgcRacGAP and ZEN-4/MKLP1 to form the centralspindlin complex. Mol Biol Cell. 2007; 18(12):4992-5003.

4. White EA, Glotzer M. Centralspindlin: at the heart of cytokinesis. Cytoskeleton. 2012; 69(11):882-892.

5. Gambale A, Iolascon A, Andolfo I, Russo R. Diagnosis and management of congenital dyserythropoietic anemias. Expert Rev Hematol. 2016; 9(3):283-296.

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