Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.
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De novo mutation in the NOTCH3 gene causing CADASIL.Acute confusional migraine: a variant not to be missedClinical variability of the cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy phenotype in two siblings of a large family showing the same mutationNeoplastic lesions in CADASIL syndrome: report of an autopsied Japanese case.
P2860
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in an Israeli family.
description
2011 nî lūn-bûn
@nan
2011 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@ast
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@en
type
label
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@ast
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@en
prefLabel
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@ast
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@en
P2860
P356
P1476
Cerebral autosomal dominant ar ...... alopathy in an Israeli family.
@en
P2093
Abdalla Bowirrat
Radi Shahien
P2860
P304
P356
10.2147/NDT.S19399
P407
P577
2011-06-20T00:00:00Z