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Paper Details

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders.
Genome Med
39
2021
HNRNP, HNRNP gene, HNRNP genes, HNRNP-related disorders, HNRNPH1, HNRNPH2, HNRNPK, HNRNPR, HNRNPU, NDD, NDD genes, NDDs, SYNCRIP, associated Mendelian genes, gene families, genes, genetic disorders, heterogeneous nuclear ribonucleoproteins, hnRNP, hnRNP-encoding genes, hnRNPs, indels, neurodevelopmental disorders, radial glial progenitors
Author NameAffiliation
Pengfei Liu
Bert B A de VriesRadboud University Medical Center
Ann NordgrenCenter for Molecular Medicine, Karolinska Institutet
Ann NordgrenKarolinska University Hospital
Enrico BertiniBambino Gesu Children's Hospital, IRCCS
Enrico BertiniBambino Gesu Children's Hospital, IRCCS
Timothy Feyma
Ghayda M MirzaaCenter for Integrative Brain Research, Seattle Children's Research Institute
Ghayda M MirzaaUniversity of Washington
Ghayda M MirzaaBrotman Baty Institute for Precision Medicine
Irene Valenzuela
Tomasz J NowakowskiUniversity of California san francisco
Tomasz J NowakowskiUniversity of California san francisco
Tomasz J NowakowskiWeill Institute for Neurosciences, University of California at San Francisco
Tomasz J NowakowskiUniversity of California san francisco
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
Evan E EichlerUniversity of Washington School of Medicine
Evan E EichlerHoward Hughes Medical Institute, University of Washington
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