Novel Human Pathological Mutations. Gene Symbol: Notch3. Disease: Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leucoencephalopathy (Cadasil).
AuthID
P-00R-T1X
P-00R-T1X
© 2024 CRACS & Inesc TEC - All Rights Reserved Privacy Policy | Terms of Service