Identification of Four Novel Candidate Genes for Non-syndromic Intellectual Disability in Pakistani Families-Reference-Cited by-同舟云学术

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Identification of Four Novel Candidate Genes for Non-syndromic Intellectual Disability in Pakistani Families

Published:2023-11-20 Issue: Volume: Page:
ISSN:0006-2928
Container-title:Biochemical Genetics
language:en
Short-container-title:Biochem Genet

Author:

Ahmed Iftikhar,Muzammal Muhammad,Khan Muzammil Ahmad,Ullah Hafiz,Farid Arshad,Yasin Muhammad,Khan Jabbar,Alam Khurshid,Mir Asif

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,General Medicine,Ecology, Evolution, Behavior and Systematics,Biochemistry

Link

https://link.springer.com/content/pdf/10.1007/s10528-023-10556-w.pdf

Reference27 articles.

1. Agrahari AK, Kumar A, Siva R et al (2018) Substitution impact of highly conserved arginine residue at position 75 in GJB1 gene in association with X-linked Charcot–Marie-tooth disease: a computational study. J Theor Biol. https://doi.org/10.1016/j.jtbi.2017.10.028

2. Agrahari AK, Pieroni E, Gatto G, Kumar A (2019) The impact of missense mutation in PIGA associated to paroxysmal nocturnal hemoglobinuria and multiple congenital anomalies-hypotonia-seizures syndrome 2: a computational study. Heliyon. https://doi.org/10.1016/j.heliyon.2019.e02709

3. Ali MZ, Farid A, Ahmad S et al (2022) In silico analysis identified putative pathogenic missense nsSNPs in human SLITRK1 gene. Genes (basel). https://doi.org/10.3390/genes13040672

4. Bonnefond L, Fender A, Rudinger-Thirion J et al (2005) Toward the full set of human mitochondrial aminoacyl-tRNA synthetases: characterization of AspRS and TyrRS. Biochemistry. https://doi.org/10.1021/bi047527z

5. Chen LQ, Hou BH, Lalonde S et al (2010) Sugar transporters for intercellular exchange and nutrition of pathogens. Nature. https://doi.org/10.1038/nature09606

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