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Novel ACTA1 mutation causes late-presenting nemaline myopat..:
Garibaldi, Matteo
;
Fattori, Fabiana
;
Pennisi, Elena Maria
...
Neuromuscular Disorders. 31 (2021) 2 - p. 139-148 , 2021
Link:
https://doi.org/10.1016/j.nmd.2020.11.012
RT Journal T1
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores
UL https://suche.suub.uni-bremen.de/peid=cr-10.1016_j.nmd.2020.11.012&Exemplar=1&LAN=DE A1 Garibaldi, Matteo A1 Fattori, Fabiana A1 Pennisi, Elena Maria A1 Merlonghi, Gioia A1 Fionda, Laura A1 Vanoli, Fiammetta A1 Leonardi, Luca A1 Bucci, Elisabetta A1 Morino, Stefania A1 Micaloni, Andrea A1 Tartaglione, Tommaso A1 Uijterwijk, Bas A1 Zierikzee, Martijn A1 Ottenheijm, Coen A1 Bertini, Enrico Silvio A1 Stoppacciaro, Antonella A1 Raffa, Salvatore A1 Salvetti, Marco A1 Antonini, Giovanni PB Elsevier BV YR 2021 SN 0960-8966 JF Neuromuscular Disorders VO 31 IS 2 SP 139 OP 148 LK http://dx.doi.org/https://doi.org/10.1016/j.nmd.2020.11.012 DO https://doi.org/10.1016/j.nmd.2020.11.012 SF ELIB - SuUB Bremen
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