NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes
- DOI
- 10.1007/s00438-022-01945-8
- Published
- 2022-08-24
- Container
- Molecular Genetics and Genomics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1007/s00438-022-01945-8,
title = {NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes},
author = {Ayaz Khan and Shixiong Tian and Muhammad Tariq and Sheraz Khan and Muhammad Safeer and Naimat Ullah and Nazia Akbar and Iram Javed and Mahnoor Asif and Ilyas Ahmad and Shahid Ullah and Humayoon Shafique Satti and Raees Khan and Muhammad Naeem and Mahwish Ali and John Rendu and Julien Fauré and Klaus Dieterich and Xenia Latypova and Shahid Mahmood Baig and Naveed Altaf Malik and Feng Zhang and Tahir Naeem Khan and Chunyu Liu},
year = {2022},
journal = {Molecular Genetics and Genomics},
doi = {10.1007/s00438-022-01945-8},
url = {https://doi.org/10.1007/s00438-022-01945-8}
}RIS
TY - JOUR TI - NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes AU - Ayaz Khan AU - Shixiong Tian AU - Muhammad Tariq AU - Sheraz Khan AU - Muhammad Safeer AU - Naimat Ullah AU - Nazia Akbar AU - Iram Javed AU - Mahnoor Asif AU - Ilyas Ahmad AU - Shahid Ullah AU - Humayoon Shafique Satti AU - Raees Khan AU - Muhammad Naeem AU - Mahwish Ali AU - John Rendu AU - Julien Fauré AU - Klaus Dieterich AU - Xenia Latypova AU - Shahid Mahmood Baig AU - Naveed Altaf Malik AU - Feng Zhang AU - Tahir Naeem Khan AU - Chunyu Liu PY - 2022 JO - Molecular Genetics and Genomics DO - 10.1007/s00438-022-01945-8 UR - https://doi.org/10.1007/s00438-022-01945-8 ER -
APA
Khan, A., Tian, S., Tariq, M., Khan, S., Safeer, M., Ullah, N., Akbar, N., Javed, I., Asif, M., Ahmad, I., Ullah, S., Satti, H. S., Khan, R., Naeem, M., Ali, M., Rendu, J., Fauré, J., Dieterich, K., Latypova, X., Baig, S. M., Malik, N. A., Zhang, F., Khan, T. N., & Liu, C. (2022). NGS-driven molecular diagnosis of heterogeneous hereditary neurological disorders reveals novel and known variants in disease-causing genes. Molecular Genetics and Genomics. https://doi.org/10.1007/s00438-022-01945-8
Source records
- crossref · retrieved 2026-09-25T16:23:59.809Z