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        "title": "Complete cDNA sequence encoding human beta-galactoside alpha-2,6-sialyltransferase.",
        "journal": "Nucleic Acids Res.",
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    {
        "title": "Refractory epilepsy and mitochondrial dysfunction due to GM3 synthase deficiency.",
        "journal": "European journal of human genetics : EJHG",
        "date": "2013-05",
        "authors": "Fragaki Konstantina, Ait-El-Mkadem Samira, Chaussenot Annabelle, Gire Catherine, Mengual Raymond, Bonesso Laurent, B\u00e9n\u00e9teau Marie, Ricci Jean-Ehrland, Desquiret-Dumas Val\u00e9rie, Procaccio Vincent, R\u00f6tig Agn\u00e8s, Paquis-Flucklinger V\u00e9ronique",
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    {
        "title": "A mutation in a ganglioside biosynthetic enzyme, ST3GAL5, results in salt & pepper syndrome, a neurocutaneous disorder with altered glycolipid and glycoprotein glycosylation.",
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        "title": "GM3 synthase deficiency due to ST3GAL5 variants in two Korean female siblings: Masquerading as Rett syndrome-like phenotype.",
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        "authors": "Mahmood Athraa Ali, Abbas Raghad Fadhil, Hussein Hashim Mueen",
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