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    Fam Cancer. 2011 Mar;10(1):127-32.

    Identification of a large rearrangement in CYLD as a cause of familial cylindromatosis.

    van den Ouweland AM, Elfferich P, Lamping R, van de Graaf R, van Veghel-Plandsoen MM, Franken SM, Houweling AC.

    Source

    Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands. a.vandenouweland@erasmusmc.nl

    Abstract

    Pathogenic mutations in CYLD can be identified in patients affected with Brooke-Spiegler syndrome, (Familial) Cylindromatosis or multiple familial trichoepithelioma. To date, only technologies which are able to identify small point mutations in CYLD, such as sequence and WAVE analysis, were used. Here we describe the identification of a larger rearrangement identified by Quantitative PCR analysis of CYLD, indicating that a combination of these technologies is necessary when searching for pathogenic mutations in CYLD.

    PMID:
    20972631
    [PubMed - indexed for MEDLINE]
    PMCID:
    PMC3036809
    Free PMC Article

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