Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability
- DOI
- 10.3389/fgene.2022.878274
- Published
- 2022-04-28
- Container
- Frontiers in Genetics
- Publisher
- Frontiers Media SA
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3389/fgene.2022.878274,
title = {Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability},
author = {Ahmed Waqas and Anam Nayab and Shabnam Shaheen and Safdar Abbas and Muhammad Latif and Misbahuddin M. Rafeeq and Ibtesam S. Al-Dhuayan and Amany I. Alqosaibi and Mashael M. Alnamshan and Ziaullah M. Sain and Alaa Hamed Habib and Qamre Alam and Muhammad Umair and Muhammad Arif Nadeem Saqib},
year = {2022},
journal = {Frontiers in Genetics},
doi = {10.3389/fgene.2022.878274},
url = {https://doi.org/10.3389/fgene.2022.878274}
}RIS
TY - JOUR TI - Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability AU - Ahmed Waqas AU - Anam Nayab AU - Shabnam Shaheen AU - Safdar Abbas AU - Muhammad Latif AU - Misbahuddin M. Rafeeq AU - Ibtesam S. Al-Dhuayan AU - Amany I. Alqosaibi AU - Mashael M. Alnamshan AU - Ziaullah M. Sain AU - Alaa Hamed Habib AU - Qamre Alam AU - Muhammad Umair AU - Muhammad Arif Nadeem Saqib PY - 2022 JO - Frontiers in Genetics DO - 10.3389/fgene.2022.878274 UR - https://doi.org/10.3389/fgene.2022.878274 ER -
APA
Waqas, A., Nayab, A., Shaheen, S., Abbas, S., Latif, M., Rafeeq, M. M., Al-Dhuayan, I. S., Alqosaibi, A. I., Alnamshan, M. M., Sain, Z. M., Habib, A. H., Alam, Q., Umair, M., & Saqib, M. A. N. (2022). Case Report: Biallelic Variant in the tRNA Methyltransferase Domain of the AlkB Homolog 8 Causes Syndromic Intellectual Disability. Frontiers in Genetics. https://doi.org/10.3389/fgene.2022.878274
Source records
- crossref · retrieved 2026-09-27T03:09:33.176Z