Mining local exome and HLA data to characterize pharmacogenetic variants in Saudi Arabia
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s00439-023-02628-z.pdf
Reference53 articles.
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2. Alali M, Ismail Al-Khalil W, Rijjal S, Al-Salhi L, Saifo M, Youssef LA (2022) Frequencies of CYP2D6 genetic polymorphisms in Arab populations. Hum Genom 16:6. https://doi.org/10.1186/s40246-022-00378-z
3. Aldahmesh MA, Khan AO, Meyer BF, Alkuraya FS (2009) Mutational spectrum of SLC4A11 in autosomal recessive CHED in Saudi Arabia. Invest Ophthalmol vis Sci 50:4142–4145. https://doi.org/10.1167/iovs.08-3006
4. Al-Dosari MS, Al-Jenoobi FI, Alkharfy KM, Alghamdi AM, Bagulb KM, Parvez MK, Al-Mohizea AM, Al-Muhsen S, Halwani R (2013) High prevalence of CYP2D6*41 (G2988A) allele in Saudi Arabians. Environ Toxicol Pharmacol 36:1063–1067. https://doi.org/10.1016/j.etap.2013.09.008
5. Alfraih F, Alawwami M, Aljurf M, Alhumaidan H, Alsaedi H, El Fakih R, Alotaibi B, Rasheed W, Bernas SN, Massalski C (2021) High-resolution HLA allele and haplotype frequencies of the Saudi Arabian population based on 45,457 individuals and corresponding stem cell donor matching probabilities. Hum Immunol 82:97–102
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