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PAH DEFICIENT PATHOLOGY IN HUMANIZED c.1066-11G>A PHENYLKETONURIA MICE

2023-11-05

Abstract excerpt

We have generated using CRISPR/Cas9 technology a partially humanized mouse model of the neurometabolic disease phenylketonuria (PKU), carrying the highly prevalent PAH variant c.1066-11G>A. This variant creates an alternative 3’ splice site, leading to the inclusion of 9 nucleotides coding for 3 extra amino acids between Q355 and Y356 of the protein. Homozygous Pah c.1066-11A mice, with a partially humanized int...

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Identifiers and source

Literature Corpus work
10c8cbd9-6827-5a4b-adcb-563d75130f4e
DOI
10.1101/2023.11.03.565447
Open publication

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PAH DEFICIENT PATHOLOGY IN HUMANIZED c.1066-11G>A PHENYLKETONURIA MICEDOI 10.1101/2023.11.03.565447
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