Nardella, Marta
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Missense mutations of CACNA1A are a frequent cause of autos..:

Travaglini, Lorena ; Nardella, Marta ; Bellacchio, Emanuele...
European Journal of Paediatric Neurology.  21 (2017)  3 - p. 450-456 , 2017
 
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9

A novel PMCA3 mutation in an ataxic patient with hypomorphi..:

Vicario, Mattia ; Calì, Tito ; Cieri, Domenico...
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.  1863 (2017)  12 - p. 3303-3312 , 2017
 
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