A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.
- DOI
- 10.1590/1678-4685-gmb-2025-0020
- Published
- 2026
- Container
- Genetics and molecular biology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1590/1678-4685-gmb-2025-0020,
title = {A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.},
author = {Fatima S and Sun D and Han J and Qiu M and Ahmad S and Zubair M and Ali MZ and Abbas S and Shafiq M and Muzammal M and Gul H and Khan J and Du S and Khan MA},
year = {2026},
journal = {Genetics and molecular biology},
doi = {10.1590/1678-4685-gmb-2025-0020},
url = {https://doi.org/10.1590/1678-4685-gmb-2025-0020}
}RIS
TY - JOUR TI - A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family. AU - Fatima S AU - Sun D AU - Han J AU - Qiu M AU - Ahmad S AU - Zubair M AU - Ali MZ AU - Abbas S AU - Shafiq M AU - Muzammal M AU - Gul H AU - Khan J AU - Du S AU - Khan MA PY - 2026 JO - Genetics and molecular biology DO - 10.1590/1678-4685-gmb-2025-0020 UR - https://doi.org/10.1590/1678-4685-gmb-2025-0020 ER -
APA
S, F., D, S., J, H., M, Q., S, A., M, Z., MZ, A., S, A., M, S., M, M., H, G., J, K., S, D., & MA, K. (2026). A novel protein truncating mutation of TTC8 causes Bardet-Biedl Syndrome (BBS) in a Pakistani family.. Genetics and molecular biology. https://doi.org/10.1590/1678-4685-gmb-2025-0020
Source records
- pubmed · retrieved 2026-09-26T10:22:27.731Z