Correction: Correlating SFTPC gene variants to interstitial lung disease in Egyptian children.

Autor: Abdel Megeid AK; Pediatric Department, Cairo University, Giza, Egypt., Refeat MM; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Ashaat EA; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Kamah G; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., El-Saiedi SA; Pediatric Department, Cairo University, Giza, Egypt., Elfalaki MM; Pediatric Department, Cairo University, Giza, Egypt., El Ruby MO; Clinical Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt., Amr KS; Medical Molecular Genetics Department, Human Genetics and Genome Research Institute, National Research Centre, Cairo, Egypt. khalda_nrc@yahoo.com.
Jazyk: angličtina
Zdroj: Journal, genetic engineering & biotechnology [J Genet Eng Biotechnol] 2022 Sep 21; Vol. 20 (1), pp. 137. Date of Electronic Publication: 2022 Sep 21.
DOI: 10.1186/s43141-022-00420-6
Databáze: MEDLINE
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