Literature DB >> 17879447

Novel human pathological mutations. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL).

Susana Ferreira1, Paulo Fontoura, Rui Guerreiro, João Paulo Oliveira.   

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Year:  2007        PMID： 17879447

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


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  2 in total

1.  NOTCH3 mutations in a cohort of Portuguese patients within CADASIL spectrum phenotype.

Authors:  Maria Rosário Almeida; Inês Elias; Carolina Fernandes; Rita Machado; Orlando Galego; Gustavo Santo
Journal:  Neurogenetics       Date:  2021-12-01       Impact factor: 2.660

2.  Vascular cognitive impairment associated with NOTCH3 Exon 33 mutation: A case report.

Authors:  Yong Sun; Yan-Jun Wei; Ying Xing
Journal:  Medicine (Baltimore)       Date:  2019-08       Impact factor: 1.817
  2 in total

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