Publication | Closed Access
High recurrence of the R1006C NOTCH3 mutation in central Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
16
Citations
14
References
2009
Year
MedicineR1006c Notch3 MutationCentral Italian PatientsNeurologyHigh RecurrenceNeuropathologyStrokeNeurovascular Disease
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