Corrigendum to “Defining the molecular pathology and consequent phenotypes in Egyptian HB patients” [J. Genet. Eng. Biotechnol. 19(1) (2021) 75]
Main Authors: | Ghada Y. El-Kamah, Rehab M. Mosaad, Mohamed B. Taher, Khalda S. Amr |
---|---|
Format: | Article |
Language: | English |
Published: |
SpringerOpen
2024-06-01
|
Series: | Journal of Genetic Engineering and Biotechnology |
Online Access: | http://www.sciencedirect.com/science/article/pii/S1687157X24000775 |
Similar Items
-
Genomic alterations in the F8 gene correlating with severe hemophilia A in Egyptian patients
by: Rehab M. Mosaad, et al.
Published: (2021-02-01) -
Whole exome sequencing identifies a new mutation in the SLC19A2 gene leading to thiamine‐responsive megaloblastic anemia in an Egyptian family
by: Khalda Amr, et al.
Published: (2019-07-01) -
Outlining the Clinical Profile of <i>TCIRG1 14 Variants</i> including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families
by: Ghada Y. El-Kamah, et al.
Published: (2023-04-01) -
Corrigendum to: “Farnesoid X receptor (FXR): Structures and ligands” [Comput. Struct. Biotechnol. J. 19 (2021) 2148–2159]
by: Longying Jiang, et al.
Published: (2022-01-01) -
Mutational spectrum of NF1 gene in 24 unrelated Egyptian families with neurofibromatosis type 1
by: Nahla N.Abdel‐Aziz, et al.
Published: (2021-12-01)