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Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.
Mol Genet Metab. 2011 Jul;103(3):303-4. doi: 10.1016/j.ymgme.2011.04.002. Epub 2011 Apr 8.
Mol Genet Metab. 2011.
PMID: 21514860
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia.
Smaili I, Hajjaj I, Razine R, Tibar H, Salmi A, Bouslam N, Moussa A, Regragui W, Bouhouche A.
Smaili I, et al.
Case Rep Genet. 2020 Dec 3;2020:8813344. doi: 10.1155/2020/8813344. eCollection 2020.
Case Rep Genet. 2020.
PMID: 33343949
Free PMC article.
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Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.
Ben El Haj R, Salmi A, Regragui W, Moussa A, Bouslam N, Tibar H, Benomar A, Yahyaoui M, Bouhouche A.
Ben El Haj R, et al.
PLoS One. 2017 Jul 19;12(7):e0181335. doi: 10.1371/journal.pone.0181335. eCollection 2017.
PLoS One. 2017.
PMID: 28723952
Free PMC article.
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Arterial stiffness, inflammatory and pro-atherogenic markers in gestational diabetes mellitus.
Salmi AA, Zaki NM, Zakaria R, Nor Aliza AG, Rasool AH.
Salmi AA, et al.
Vasa. 2012 Mar;41(2):96-104. doi: 10.1024/0301-1526/a000171.
Vasa. 2012.
PMID: 22403127
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