Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses
- DOI
- 10.1111/ahg.70061
- Published
- 2026-09-21
- Container
- Annals of Human Genetics
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1111/ahg.70061,
title = {Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses},
author = {Zafar Ali and Najeeb Ullah and Muneeba Bibi and Sania Fawad and Sana Khan and Mansoor Ali and Irum Hassan and Sana Fazal and Fazal Akbar and Shahid Baig and Niklas Dahl},
year = {2026},
journal = {Annals of Human Genetics},
doi = {10.1111/ahg.70061},
url = {https://doi.org/10.1111/ahg.70061}
}RIS
TY - JOUR TI - Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses AU - Zafar Ali AU - Najeeb Ullah AU - Muneeba Bibi AU - Sania Fawad AU - Sana Khan AU - Mansoor Ali AU - Irum Hassan AU - Sana Fazal AU - Fazal Akbar AU - Shahid Baig AU - Niklas Dahl PY - 2026 JO - Annals of Human Genetics DO - 10.1111/ahg.70061 UR - https://doi.org/10.1111/ahg.70061 ER -
APA
Ali, Z., Ullah, N., Bibi, M., Fawad, S., Khan, S., Ali, M., Hassan, I., Fazal, S., Akbar, F., Baig, S., & Dahl, N. (2026). Exome Sequencing Identifies Novel Variants Causing Hearing Loss in Three Consanguineous Pakistani Families: Insights From Genomics and Bioinformatics Analyses. Annals of Human Genetics. https://doi.org/10.1111/ahg.70061
Source records
- crossref · retrieved 2026-09-24T18:57:55.785Z