Work

[NOTCH3 gene mutations in four Chinese families with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy].

Year: 2004
Type: article
Source: PubMed
Language: English
Subfield: Neurology
Field: Medicine
Open Access status: closed
OpenAlex ID: W48866158
FWCI: 0.683
Cites:
Cited by: 7
Related to: 10