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  • Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

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Research Article
Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

Authors

    Citation

    Ala-Mello S, Sankila EM, Koskimies O, et al
    Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.
    Journal of Medical Genetics 1998;35:279-283.

    Publication history

    • First published April 1, 1998.
    Online issue publication 
    April 27, 2016

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