Human Genome Epidemiology Literature Finder
Rare Diseases
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Query Trace: Aicardi Syndrome[original query] |
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Mutational spectrum of CDKL5 in early-onset encephalopathies: a study of a large collection of French patients and review of the literature. Clinical genetics 2009 Oct 76 (4): 357-71. Nemos C, Lambert L, Giuliano F, Doray B, Roubertie A, Goldenberg A, Delobel B, Layet V, N'guyen M A, Saunier A, Verneau F, Jonveaux P, Philippe |
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