Literature DB >> 17879433

Novel human pathological mutations. Gene symbol: APOB. Disease: normotriglyceridemic hypobetalipoproteinemia.

Vivienne Homer1, Peter M George, Stephen du Toit, James S Davidson, Callum J Wilson.   

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Year:  2007        PMID： 17879433

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


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  3 in total

1.  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

Review 2.  Genetic Factors of Cerebral Small Vessel Disease and Their Potential Clinical Outcome.

Authors:  Vo Van Giau; Eva Bagyinszky; Young Chul Youn; Seong Soo A An; Sang Yun Kim
Journal:  Int J Mol Sci       Date:  2019-09-03       Impact factor: 5.923

Review 3.  Systematic Review of Cysteine-Sparing NOTCH3 Missense Mutations in Patients with Clinical Suspicion of CADASIL.

Authors:  Elena Muiño; Cristina Gallego-Fabrega; Natalia Cullell; Caty Carrera; Nuria Torres; Jurek Krupinski; Jaume Roquer; Joan Montaner; Israel Fernández-Cadenas
Journal:  Int J Mol Sci       Date:  2017-09-13       Impact factor: 5.923
  3 in total

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