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 Vol 9: Deletion of Prepl Causes Growth Impairment and Hypotonia in Mice.


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This article is from PLoS ONE, volume 9.AbstractGenetic studies of rare diseases can identify genes of unknown function that strongly impact human physiology. Prolyl endopeptidase-like (PREPL) is an uncharacterized member of the prolyl peptidase family that was discovered because of its deletion in humans with hypotonia-cystinuria syndrome (HCS). H

Autor: Lone, Anna Mari; Leidl, Mathias; McFedries, Amanda K.; Horner, James W.; Creemers, John; Saghatelian, Alan

Fuente: https://archive.org/







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