Hypogammaglobulinemia with T‐cell defects and autoimmune manifestations associated with chromosome 15q24 microdeletion-Reference-Cited by-同舟云学术

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Hypogammaglobulinemia with T‐cell defects and autoimmune manifestations associated with chromosome 15q24 microdeletion

Published:2023-08-22 Issue:6 Volume:98 Page:
ISSN:0300-9475
Container-title:Scandinavian Journal of Immunology
language:en
Short-container-title:Scand J Immunol

Author:

Honkanen Meeri¹^ORCID,Otava Ulla¹,Viskari Hanna¹,Rantala Sari¹,Outinen Tuula¹,Toiminen Heidi²,Syrjänen Jaana¹

Affiliation:

1. Department of Internal Medicine, Tampere University Hospital and Faculty of Medicine and Life Sciences Tampere University Tampere Finland

2. Department of Clinical Genetics, Tampere University Hospital and Faculty of Medicine and Life Sciences Tampere University Tampere Finland

Publisher

Wiley

Subject

Immunology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/sji.13324

Reference6 articles.

1. Chromosome 15q24 microdeletion syndrome

2. Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders

3. Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability

4. NEIL1 is a candidate gene associated with common variable immunodeficiency in a patient with a chromosome 15q24 deletion

5. Further clinical and molecular delineation of the 15q24 microdeletion syndrome

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