Alfredo Brusco
Università degli Studi di Torino
117 papers found
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Identification of the DNA methylation signature of Mowat-Wilson syndrome
UploadHeterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
UploadMotor and cognitive outcomes of cerebello-spinal stimulation in neurodegenerative ataxia
UploadMissense variant contribution to USP9X-female syndrome
Download from www.nature.comCover Image, Volume 170A, Number 7, July 2016
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