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A novel homozygous SACS mutation identified by whole exome sequencing-genotype phenotype correlations of all published cases. [electronic resource] by
- Xiromerisiou, Georgia
- Dadouli, Katerina
- Marogianni, Chrysoula
- Provatas, Antonios
- Ntellas, Panagiotis
- Rikos, Dimitrios
- Stathis, Pantelis
- Georgouli, Despina
- Loules, Gedeon
- Zamanakou, Maria
- Hadjigeorgiou, Georgios M
Producer: 20201008
In:
Journal of molecular neuroscience : MN vol. 70
Availability: No items available.
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