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Browsing by Author Hough, Tertius

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Next-generation sequencing to dissect hereditary nephrotic syndrome in mice identifies a hypomorphic mutation in Lamb2 and models Pierson's syndrome

Author(s)Bull, Katherine R; Mason, Thomas; Rimmer, Andrew J., et al
TypeJournal article
Date Published2014
Date Created-

Upregulation of PKD1L2 provokes a complex neuromuscular disease in the mouse

Author(s)Mackenzie, Francesca E; Romero, Rosario; Williams, Debbie, et al
TypeJournal article
Date Published2009
Date Created-
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