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UBTF Mutation Causes Complex Phenotype of Neurodegeneration and Severe Epilepsy in Childhood. [electronic resource] by
- Sedláčková, Lucie
- Laššuthová, Petra
- Štěrbová, Katalin
- Haberlová, Jana
- Vyhnálková, Emílie
- Neupauerová, Jana
- Staněk, David
- Šedivá, Marie
- Kršek, Pavel
- Seeman, Pavel
Producer: 20191230
In:
Neuropediatrics vol. 50
Availability: No items available.
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Two Novel Variants Affecting CDKL5 Transcript Associated with Epileptic Encephalopathy. [electronic resource] by
- Neupauerová, Jana
- Štěrbová, Katalin
- Vlčková, Markéta
- Sebroňová, Věra
- Maříková, Tat'ána
- Krůtová, Marcela
- David, Staněk
- Kršek, Pavel
- Žaliová, Markéta
- Seeman, Pavel
- Laššuthová, Petra
Producer: 20180206
In:
Genetic testing and molecular biomarkers vol. 21
Availability: No items available.
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