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2003 1
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2013 1
2014 2
2015 2
2016 4
2018 3
2019 1
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2024 1

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Page 1
Mitochondrial DNA maintenance defects: potential therapeutic strategies.
Almannai M, El-Hattab AW, Azamian MS, Ali M, Scaglia F. Almannai M, et al. Among authors: ali m. Mol Genet Metab. 2022 Sep-Oct;137(1-2):40-48. doi: 10.1016/j.ymgme.2022.07.003. Epub 2022 Jul 6. Mol Genet Metab. 2022. PMID: 35914366 Free PMC article. Review.
Clinical trials in mitochondrial disorders, an update.
Almannai M, El-Hattab AW, Ali M, Soler-Alfonso C, Scaglia F. Almannai M, et al. Among authors: ali m. Mol Genet Metab. 2020 Sep-Oct;131(1-2):1-13. doi: 10.1016/j.ymgme.2020.10.002. Epub 2020 Oct 6. Mol Genet Metab. 2020. PMID: 33129691 Free PMC article. Review.
Novel sequencing technologies to support industrial biotechnology.
Costessi A, van den Bogert B, May A, Ver Loren van Themaat E, Roubos JA, Kolkman MAB, Butler D, Pirovano W. Costessi A, et al. Among authors: may a. FEMS Microbiol Lett. 2018 Aug 1;365(16). doi: 10.1093/femsle/fny103. FEMS Microbiol Lett. 2018. PMID: 30010862 Review.
The complex behavioral phenotype of 15q13.3 microdeletion syndrome.
Ziats MN, Goin-Kochel RP, Berry LN, Ali M, Ge J, Guffey D, Rosenfeld JA, Bader P, Gambello MJ, Wolf V, Penney LS, Miller R, Lebel RR, Kane J, Bachman K, Troxell R, Clark G, Minard CG, Stankiewicz P, Beaudet A, Schaaf CP. Ziats MN, et al. Among authors: ali m. Genet Med. 2016 Nov;18(11):1111-1118. doi: 10.1038/gim.2016.9. Epub 2016 Mar 10. Genet Med. 2016. PMID: 26963284 Free article.
22 results