Divergent Features of Mitochondrial Deficiencies in LGMD2A Associated With Novel Calpain-3 Mutations
El-Khoury, Riyad, Traboulsi, Sahar, Hamad, Tarek, Lamaa, Maher, Sawaya, Raja, Ahdab-Barmada, Mamdouha
Published in Journal of neuropathology and experimental neurology (01.01.2019)
Published in Journal of neuropathology and experimental neurology (01.01.2019)
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Contribution of next generation sequencing in pediatric practice in Lebanon. A Study on 213 cases
Nair, Pratibha, Sabbagh, Sandra, Mansour, Hicham, Fawaz, Ali, Hmaimess, Ghassan, Noun, Peter, Dagher, Rawane, Megarbane, Hala, Hana, Sayeeda, Alame, Saada, Lamaa, Maher, Hasbini, Dana, Farah, Roula, Rajab, Mariam, Stora, Samantha, El‐Tourjuman, Oulfat, Abou Jaoude, Pauline, Chalouhi, Gihad, Sayad, Rony, Gillart, Anne‐Celine, Al‐Ali, Mahmoud, Delague, Valerie, El‐Hayek, Stephany, Mégarbané, André
Published in Molecular genetics & genomic medicine (01.11.2018)
Published in Molecular genetics & genomic medicine (01.11.2018)
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