Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)-Reference-Cited by-同舟云学术

Hematologically important mutations: The autosomal forms of chronic granulomatous disease (third update)

Published:2021-12 Issue: Volume:92 Page:102596
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Roos Dirk,van Leeuwen Karin,Hsu Amy P.,Priel Debra Long,Begtrup Amber,Brandon Rhonda,Rawat Amit,Vignesh Pandiarajan,Madkaikar Manesha,Stasia Marie José,Bakri Faris Ghalib,de Boer Martin,Roesler Joachim,Köker Nezihe,Köker M. Yavuz,Jakobsen Marianne,Bustamante Jacinta,Garcia-Morato Maria Bravo,Shephard Juan Luis Valdivieso,Cagdas Deniz,Tezcan Ilhan,Sherkat Roya,Mortaz Esmaeil,Fayezi Abbas,Shahrooei Mohammad,Wolach Baruch,Blancas-Galicia Lizbeth,Kanegane Hirokazu,Kawai Toshinao,Condino-Neto Antonio,Vihinen Mauno,Zerbe Christa S.,Holland Steven M.,Malech Harry L.,Gallin John I.,Kuhns Douglas B.

Funder

University Grenoble Alpes

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference110 articles.

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2. Hematologically important mutations: X-linked chronic granulomatous disease (third update);Roos;Blood Cells Mol. Dis.,2010

3. A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity;Matute;Blood,2009

4. Inherited p40phox deficiency differs from classic chronic granulomatous disease;van de Geer;J. Clin. Invest.,2018

5. A homozygous loss-of-function mutation leading to CYBC1 deficiency causes chronic granulomatous disease;Arnadottir;Nat. Commun.,2018

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