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The milder phenotype of the dystrophin gene double deletions.
El-Harouni AA, Amr KS, Effat LK, Eassawi ML, Ismail S, Gad YZ, El-Awady MK. El-Harouni AA, et al. Among authors: amr ks. Acta Neurol Scand. 2003 Jun;107(6):400-4. doi: 10.1034/j.1600-0404.2003.00072.x. Acta Neurol Scand. 2003. PMID: 12757471
A novel mutation in the leptin gene (W121X) in an Egyptian family.
Mazen I, Amr K, Tantawy S, Farooqi IS, El Gammal M. Mazen I, et al. Among authors: amr k. Mol Genet Metab Rep. 2014 Nov 11;1:474-476. doi: 10.1016/j.ymgmr.2014.10.002. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896126 Free PMC article.
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