E. Flachsová
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Molecular Diagnostics of Copper-Transporting Protein Mutations Allows Early Onset Individual Therapy of Menkes Disease
L. Králík, E. Flachsová, H. Hansíková, V. Saudek, J. Zeman, Pavel Martásek
2017, Vol. 63, Issue 5-6, pp. 165-173 -
A New Mutation within the Porphobilinogen Deaminase Gene Leading to a Truncated Protein as a Cause of Acute Intermittent Porphyria in an Extended Indian Family
E. Flachsová, I. C. Verma, D. Ulbrichová, R. Saxena, J. Zeman, V. Saudek, C. S. Raman, Pavel Martásek
2007, Vol. 53, Issue 6, pp. 194-201
