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A murine model of hnRNPH2-related neurodevelopmental disorder recapitulates clinical features of human disease and reveals a mechanism for genetic compensation of HNRNPH2
Ane Korff, Xiaojing Yang, Kevin O’Donovan, Fen Yang, Tushar Patni, Heather Tillman, Abner Gonzalez, Yuh Min Chook, J. Paul Taylor, Hong Joo Kim
doi: https://doi.org/10.1101/2022.03.17.484791
Ane Korff
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Xiaojing Yang
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Kevin O’Donovan
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Fen Yang
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Tushar Patni
2Department of Biostatistics, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Heather Tillman
3Department of Pathology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
Abner Gonzalez
4Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA
Yuh Min Chook
4Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas, TX, USA
J. Paul Taylor
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA
5Howard Hughes Medical Institute, Chevy Chase, Maryland, USA
Hong Joo Kim
1Department of Cell and Molecular Biology, St. Jude Children’s Research Hospital, Memphis, Tennessee, USA

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Posted March 19, 2022.
A murine model of hnRNPH2-related neurodevelopmental disorder recapitulates clinical features of human disease and reveals a mechanism for genetic compensation of HNRNPH2
Ane Korff, Xiaojing Yang, Kevin O’Donovan, Fen Yang, Tushar Patni, Heather Tillman, Abner Gonzalez, Yuh Min Chook, J. Paul Taylor, Hong Joo Kim
bioRxiv 2022.03.17.484791; doi: https://doi.org/10.1101/2022.03.17.484791
A murine model of hnRNPH2-related neurodevelopmental disorder recapitulates clinical features of human disease and reveals a mechanism for genetic compensation of HNRNPH2
Ane Korff, Xiaojing Yang, Kevin O’Donovan, Fen Yang, Tushar Patni, Heather Tillman, Abner Gonzalez, Yuh Min Chook, J. Paul Taylor, Hong Joo Kim
bioRxiv 2022.03.17.484791; doi: https://doi.org/10.1101/2022.03.17.484791
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