A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death-Reference-Cited by-同舟云学术

A homozygous variant in ABCA3 is associated with severe respiratory distress and early neonatal death

Published:2021-08-18 Issue:6 Volume:61 Page:231-233
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenit Anom

Author:

Al‐Iede Montaha¹^ORCID,Khanfar Mariam²^ORCID,Srour Luma³^ORCID,Rabah Raja⁴^ORCID,Al‐Abbadi Mousa³^ORCID,Azab Bilal³^ORCID,Badran Eman F.¹^ORCID

Affiliation:

1. Department of Pediatrics, School of Medicine The University of Jordan Amman Jordan

2. Department of Medical Laboratory Sciences Jordan University of Science and Technology Irbid Jordan

3. Department of Pathology, Microbiology and Forensic Medicine, School of Medicine The University of Jordan Amman Jordan

4. Department of Pathology, University of Michigan Von‐Voigtlander Women's Hospital Ann Arbor Michigan USA

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12437

Reference4 articles.

1. Genotype–Phenotype Correlations for Infants and Children with ABCA3 Deficiency

2. Molecular and cellular characteristics of ABCA3 mutations associated with diffuse parenchymal lung diseases in children

3. Novel mutation in the ATP‐binding cassette transporter A3 (ABCA3) encoding gene causes respiratory distress syndrome in a term newborn in Southwest Iran;Rezaei F;Iran J Pediatr,2016

4. The classification of ATP-binding cassette subfamily A member 3 mutations using the cystic fibrosis transmembrane conductance regulator classification system

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Case Report: Report of Two Cases of Interstitial Lung Disease Caused by Novel Compound Heterozygous Variants in the ABCA3 Gene;Frontiers in Genetics;2022-04-06