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Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)

✍ Scribed by S. Testi; G. Malerba; M. Ferrarini; M. Ragno; L. Pradotto; A. Mauro; G.M. Fabrizi

Book ID: 119304519
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 169 KB
Volume: 319
Category: Article
ISSN: 0022-510X
DOI: 10.1016/j.jns.2012.05.025

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