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Showing results for alamoudi ms[au]
Your search for Alhmoudi MS[au] retrieved no results
Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia.
Al-Hamed MH, Imtiaz F, Al-Hassnan Z, Al-Owain M, Al-Zaidan H, Alamoudi MS, Faqeih E, Alfadhel M, Al-Asmari A, Saleh MM, Almutairi F, Moghrabi N, AlSayed M. Al-Hamed MH, et al. Among authors: alamoudi ms. Mol Genet Metab Rep. 2019 Jan 9;18:22-29. doi: 10.1016/j.ymgmr.2018.12.004. eCollection 2019 Mar. Mol Genet Metab Rep. 2019. PMID: 30705822 Free PMC article.
Carnitine palmityl transferase I deficiency.
Al-Aqeel AI, Rashed MS, Ruiter JP, Al-Husseini HF, Al-Amoudi MS, Wanders RJ. Al-Aqeel AI, et al. Saudi Med J. 2001 Nov;22(11):1025-9. Saudi Med J. 2001. PMID: 11744980