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M Cervenková

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Blood Cells, Molecules & Diseases|April 1, 2000
Analysis of the beta-glucocerebrosidase gene in Czech and Slovak Gaucher patients: mutation profile and description of six novel mutant allelesK Hodanová, M Hrebícek, M Cervenková, et al.
Human Molecular Genetics|April 20, 2001
A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulationH Hulková, M Cervenková, J Ledvinová, et al.
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Pageof 1
Blood Cells, Molecules & Diseases|April 1, 2000
Analysis of the beta-glucocerebrosidase gene in Czech and Slovak Gaucher patients: mutation profile and description of six novel mutant allelesK Hodanová, M Hrebícek, M Cervenková, et al.
Human Molecular Genetics|April 20, 2001
A novel mutation in the coding region of the prosaposin gene leads to a complete deficiency of prosaposin and saposins, and is associated with a complex sphingolipidosis dominated by lactosylceramide accumulationH Hulková, M Cervenková, J Ledvinová, et al.
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