A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis

Christopher Esapa, Rosie Head, Gethin Thomas, Matthew Brown, Peter Croucher, Roger Cox, Steve Brown, Rajesh Thakker

    Research output: Other contribution to conference › Abstract

    Abstract

    Kyphosis is a common spinal disorder affecting up to 8.3% of the population, and associated with significant morbidity. Familial and twin studies have implicated a genetic involvement. However, the causative genes have not been identified.
    Original languageEnglish
    Pages25
    Number of pages1
    Publication statusPublished - 2011
    EventSociety for Endocrinology BES 2010 - Manchester, United Kingdom
    Duration: 14 Mar 2010 → 17 Mar 2010
    https://web.archive.org/web/20100403001113/http://www.endocrinology.org:80/meetings/2010/SFEBES2010/

    Conference

    ConferenceSociety for Endocrinology BES 2010
    CountryUnited Kingdom
    CityManchester
    Period14/03/10 → 17/03/10
    Internet address

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    Esapa, C., Head, R., Thomas, G., Brown, M., Croucher, P., Cox, R., Brown, S., & Thakker, R. (2011). A mouse with an ENU-induced mutation (Tyr209Asn) in the natriuretic peptide receptor 3 (Npr3) develops autosomal recessive kyphosis. 25. Abstract from Society for Endocrinology BES 2010, Manchester, United Kingdom. http://www.endocrine-abstracts.org/ea/0025/ea0025OC4.1.htm