Sarka Bendova
2PUBLICATIONS
17CO-AUTHORS
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Publications (2)
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|Aug 30, 2025
Phenotype Analysis in Two Families With Otopalatodigital Syndrome Spectrum Disorder Based on FLNA Gene Variants.Martin Schwarz, Miroslav Fišer, Lenka Šodková
|Feb 25, 2023
A new patient with congenital myasthenic syndrome type 20 due to compound heterozygous missense SLC5A7 variants suggests trends in genotype-phenotype correlation.Marketa Vlckova, Darina Prchalova, Pavel Zimmermann
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Frequent Collaborators
1 joint publications
Marketa Vlckova
1 joint publications
Darina Prchalova
1 joint publications
Pavel Zimmermann
1 joint publications
Jana Haberlova
1 joint publications
Viktor Stranecky
1 joint publications
Zdenek Sedlacek
1 joint publications
Miroslava Hancarova
1 joint publications
Martin Schwarz
1 joint publications
Miroslav Fišer
1 joint publications
Lenka Šodková
