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Connection

Astrid Rasmussen to Mutation, Missense

This is a "connection" page, showing publications Astrid Rasmussen has written about Mutation, Missense.
Connection Strength

0.128
  1. Founder effect for the Ala431Glu mutation of the presenilin 1 gene causing early-onset Alzheimer's disease in Mexican families. Neurogenetics. 2006 Jul; 7(3):195-200.
    View in: PubMed
    Score: 0.064
  2. Genotype-phenotype correlations for EPM2A mutations in Lafora's progressive myoclonus epilepsy: exon 1 mutations associate with an early-onset cognitive deficit subphenotype. Hum Mol Genet. 2002 May 15; 11(11):1263-71.
    View in: PubMed
    Score: 0.049
  3. Mutations in EFHC1 cause juvenile myoclonic epilepsy. Nat Genet. 2004 Aug; 36(8):842-9.
    View in: PubMed
    Score: 0.014
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.