Cargando…
Correlating SFTPC gene variants to interstitial lung disease in Egyptian children
BACKGROUND: Interstitial lung disease (ILD) is a broad heterogeneous group of lung disorders that is characterized by inflammation of the lungs. Surfactant dysfunction disorders are a rare form of ILD diseases that result from mutations in surfactant protein C gene (SFTPC) with prevalence of approxi...
Autores principales: | Abdel Megeid, Azza K., Refeat, Miral M., Ashaat, Engy A., El-Kamah, Ghada, El-Saiedi, Sonia A., Elfalaki, Mona M., El Ruby, Mona O., Amr, Khalda S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360361/ https://www.ncbi.nlm.nih.gov/pubmed/35939165 http://dx.doi.org/10.1186/s43141-022-00399-0 |
Ejemplares similares
-
Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children
por: Abdel Megeid, Azza K., et al.
Publicado: (2022) -
New drug-like small molecule antagonizes phosphatidylinositol (3,4,5)-trisphosphate (PIP3) in patients with conotruncal heart defects
por: Fayez, Alaaeldin G., et al.
Publicado: (2023) -
miR-454-3p and miR-194-5p targeting cardiac sarcolemma ion exchange transcripts are potential noninvasive diagnostic biomarkers for childhood dilated cardiomyopathy in Egyptian patients
por: Fayez, Alaaeldin G., et al.
Publicado: (2022) -
Defining the molecular pathology and consequent phenotypes in Egyptian HB patients
por: El-Kamah, Ghada Y., et al.
Publicado: (2021) -
Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family
por: Amr, Khalda, et al.
Publicado: (2019)