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NGS in Hereditary Ataxia: When Rare Becomes Frequent:
Galatolo, Daniele
;
De Michele, Giovanna
;
Silvestri, Gabriella
...
International Journal of Molecular Sciences. 22 (2021) 16 - p. 8490 , 2021
Link:
https://doi.org/10.3390/ijms22168490
RT Journal T1
NGS in Hereditary Ataxia: When Rare Becomes Frequent
UL https://suche.suub.uni-bremen.de/peid=cr-10.3390_ijms22168490&Exemplar=1&LAN=DE A1 Galatolo, Daniele A1 De Michele, Giovanna A1 Silvestri, Gabriella A1 Leuzzi, Vincenzo A1 Casali, Carlo A1 Musumeci, Olimpia A1 Antenora, Antonella A1 Astrea, Guja A1 Barghigiani, Melissa A1 Battini, Roberta A1 Battisti, Carla A1 Caputi, Caterina A1 Cioffi, Ettore A1 De Michele, Giuseppe A1 Dotti, Maria Teresa A1 Fico, Tommasina A1 Fiorillo, Chiara A1 Galosi, Serena A1 Lieto, Maria A1 Malandrini, Alessandro A1 Melone, Marina A. B. A1 Mignarri, Andrea A1 Natale, Gemma A1 Pegoraro, Elena A1 Petrucci, Antonio A1 Ricca, Ivana A1 Riso, Vittorio A1 Rossi, Salvatore A1 Rubegni, Anna A1 Scarlatti, Arianna PB MDPI AG YR 2021 SN 1422-0067 JF International Journal of Molecular Sciences VO 22 IS 16 SP 8490 LK http://dx.doi.org/https://doi.org/10.3390/ijms22168490 DO https://doi.org/10.3390/ijms22168490 SF ELIB - SuUB Bremen
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