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Two Novel Homozygous HPS6 Mutations (Double Mutant) Identified by Whole-Exome Sequencing in a Saudi Consanguineous Family Suspected for Oculocutaneous Albinism.
Karim S, Saharti S, Alganmi N, Mirza Z, Alfares A, Turkistany S, Al-Attas M, Noureldin H, Al Sakkaf K, Abusamra H, Al-Qahtani M, Abuzenadah A. Karim S, et al. Among authors: mirza z. Life (Basel). 2021 Dec 23;12(1):14. doi: 10.3390/life12010014. Life (Basel). 2021. PMID: 35054407 Free PMC article.
Familial Screening for the Prevention of Rare Diseases: A Focus on Lipodystrophy in Southern Saudi Arabia.
Abuzenadah A, Alganmi N, AlQurashi R, Hawsa E, AlOtibi A, Hummadi A, Nahari AA, AlZelaye S, Aljuhani NR, Al-Attas M, Abusamra H, Turkistany S, Karim S, Mirza Z, Al-Qahtani M, Chaudhary A, Al Eissa MM. Abuzenadah A, et al. Among authors: mirza z. J Epidemiol Glob Health. 2024 Mar;14(1):162-168. doi: 10.1007/s44197-023-00182-5. Epub 2024 Jan 17. J Epidemiol Glob Health. 2024. PMID: 38231342 Free PMC article.
Genomic answers for recurrent spontaneous abortion in Saudi Arabia: An array comparative genomic hybridization approach.
Karim S, Jamal HS, Rouzi A, Ardawi MSM, Schulten HJ, Mirza Z, Alansari NA, Al-Quaiti MM, Abusamra H, Naseer MI, Turki R, Chaudhary AG, Gari M, Abuzenadah AM, Al-Qhatani MH. Karim S, et al. Among authors: mirza z. Reprod Biol. 2017 Jun;17(2):133-143. doi: 10.1016/j.repbio.2017.03.003. Epub 2017 Apr 18. Reprod Biol. 2017. PMID: 28431992
209 results