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dc.contributor.authorMcDonald, J. Daviden_US
dc.date.accessioned2012-01-24T17:48:29Z
dc.date.available2012-01-24T17:48:29Z
dc.date.issued2000-11en_US
dc.identifier11487255en_US
dc.identifier9204153en_US
dc.identifier.citationContemporary topics in laboratory animal science / American Association for Laboratory Animal Science. 2000 Nov; 39(6): 54-6.en_US
dc.identifier.issn1060-0558en_US
dc.identifier.urihttp://www.ingentaconnect.com/content/aalas/jaalas/2000/00000039/00000006/art00012
dc.identifier.urihttp://hdl.handle.net/10057/4124
dc.descriptionClick on the link below to access the article (may not be free).en_US
dc.description.abstractBecause of the ethical problems of withholding dietary treatment from patients with phenylketonuria, effectively studying long-term effects such as postnatal growth rates is difficult or impossible. The only literature available on the growth rate of phenylketonurics dates from the era before effective dietary treatment regimens were instituted routinely. Although some of these studies suggest that these patients have a reduced growth rate, whether this is a consistent feature of the untreated phenylketonuric is unclear. The mutant mouse line BTBR-Pahenu, a genetic model for human phenylketonuria, provides an opportunity to conduct studies that will clarify this issue. In this study, the weights of newborn mice were monitored from about 7 to 40 days after birth. Comparison to heterozygous, sex-matched littermates revealed a reduction in the size of homozygous mutants throughout the study. Therefore, reduced postnatal growth is an abiding feature of phenylketonuria in this mouse model. This finding not only helps to document the association between size reduction and untreated phenylketonuria but also sets the stage for studies designed to investigate the means by which size reduction occurs.en_US
dc.language.isoengen_US
dc.publisherAmerican Association for Laboratory Animal Scienceen_US
dc.relation.ispartofseriesContemporary topics in laboratory animal science / American Association for Laboratory Animal Scienceen_US
dc.sourceNLMen_US
dc.subjectResearch Support, U.S. Gov't, Non-P.H.S.en_US
dc.subject.meshAnimalsen_US
dc.subject.meshBody Constitutionen_US
dc.subject.meshDisease Models, Animalen_US
dc.subject.meshFemaleen_US
dc.subject.meshGrowthen_US
dc.subject.meshMaleen_US
dc.subject.meshMice/growth & developmenten_US
dc.subject.meshPhenylketonurias/complicationsen_US
dc.subject.meshPoint Mutationen_US
dc.titlePostnatal growth in a mouse genetic model of classical phenylketonuriaen_US
dc.typeArticleen_US
dc.description.versionpeer revieweden_US


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