Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). [electronic resource]
Producer: 20130212Description: 37-41 p. digitalISSN:- 1878-5883
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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