A novel mutation in SLC39A7 identified in a patient with autosomal
recessive agammaglobulinemia
- Melinda Erdős,
- Kristina Mironska,
- Lidia Kareva,
- Katarina Stavrik,
- Arijeta Hasani,
- Arpad Lanyi,
- Judit Kallai,
- Laszlo Marodi
Melinda Erdős
University of Debrecen, Faculty of Medicine
Corresponding Author:melinda.erdos@yahoo.com
Author ProfileKristina Mironska
Ss Cyril and Methodius University in Skopje
Author ProfileKatarina Stavrik
Ss Cyril and Methodius University in Skopje
Author ProfileArijeta Hasani
Ss Cyril and Methodius University in Skopje
Author Profile07 Mar 2022Submitted to Pediatric Allergy and Immunology 14 Mar 2022Reviewer(s) Assigned
05 Apr 2022Review(s) Completed, Editorial Evaluation Pending
08 Apr 2022Editorial Decision: Revise Minor
15 Apr 20221st Revision Received
18 Apr 2022Review(s) Completed, Editorial Evaluation Pending
21 Apr 2022Reviewer(s) Assigned
09 May 2022Editorial Decision: Accept
