Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities

Authors

Emily Brereton, Washington University School of Medicine in St. Louis
Emily Fassi, Washington University School of Medicine in St. Louis
Gabriel C. Araujo, St. Louis Children's Hospital
Jonathan Dodd, St. Louis Children's Hospital
Aida Telegrafi, GeneDx
Sheel J. Pathak, Washington University School of Medicine in St. Louis
Marwan Shinawi, Washington University School of Medicine in St. Louis

Journal

Molecular Genetics and Genomic Medicine

Publication Date

2018

Volume

6

Issue

2

Inclusive Pages

294-300

Document Type

Open Access Publication

DOI

10.1002/mgg3.362

Rights and Permissions

Brereton E, Fassi E, Araujo GC, et al. Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities. Mol Genet Genomic Med. 2018;6:294–300. https://doi.org/10.1002/mgg3.362 This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. © 2017 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc

Recommended Citation

Brereton, Emily; Fassi, Emily; Araujo, Gabriel C.; Dodd, Jonathan; Telegrafi, Aida; Pathak, Sheel J.; and Shinawi, Marwan, "Mutations in the PH Domain of DNM1 are associated with a nonepileptic phenotype characterized by developmental delay and neurobehavioral abnormalities." Molecular Genetics and Genomic Medicine. 6, 2. 294-300. (2018).
https://digitalcommons.wustl.edu/open_access_pubs/6856