Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry

A J Cassidy, S V Brugnatelli, C Ayuso, A Avila-Fernandez, D Zeller, Douglas H. Lester, The Tayside Centre For Genomic Analysis

    Research output: Contribution to conferencePoster

    Original languageEnglish
    Pages1398
    Number of pages1
    Publication statusPublished - 2016
    EventAmerican Society of Human Genetics conference 2016 - Vancouver Convention Centre, Vancouver, Canada
    Duration: 18 Oct 201622 Oct 2016
    http://www.ashg.org/2016meeting/

    Conference

    ConferenceAmerican Society of Human Genetics conference 2016
    Abbreviated titleASHG 2016
    CountryCanada
    CityVancouver
    Period18/10/1622/10/16
    Internet address

    Cite this

    Cassidy, A. J., Brugnatelli, S. V., Ayuso, C., Avila-Fernandez, A., Zeller, D., Lester, D. H., & The Tayside Centre For Genomic Analysis (2016). Exome sequencing and subsequent haplotype analysis of a Scottish Cone-Rod patient, homozygous for a common “Spanish” CERKL mutation, points towards a distant common ancestry. 1398. Poster session presented at American Society of Human Genetics conference 2016, Vancouver, Canada.