Journal
Brain Communications
Publication Date
1-1-2024
Volume
6
Issue
6
First Page
fcae377
Document Type
Open Access Publication
DOI
10.1093/braincomms/fcae377
Rights and Permissions
Sara Nagy, Alistair T Pagnamenta, Elisa Cali, Hilde M H Braakman, Juerd Wijntjes, Benno Kusters, Marc Gotkine, Orly Elpeleg, Vardiella Meiner, Jerica Lenberg, Kristen Wigby, Jennifer Friedman, Luke D Perry, Alexander M Rossor, Anna Uhrova Meszarosova, Dana Thomasova, Saiju Jacob, Mary O'Driscoll, Lenika De Simone, Dorothy K Grange, Richard Sommerville, Zahra Firoozfar, Shahryar Alavi, Mahta Mazaheri, Jevin M Parmar, Phillipa J Lamont, Veronica Pini, Anna Sarkozy, Francesco Muntoni, Gianina Ravenscroft, Eppie Jones, Declan O'Rourke, Melissa Nel, Jeannine M Heckmann, Michelle Kvalsund, Musambo M Kapapa, Somwe Wa Somwe, David R Bearden, Arman Çakar, Anne-Marie Childs, Rita Horvath, Mary M Reilly, Henry Houlden, Reza Maroofian, Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations, Brain Communications, Volume 6, Issue 6, 2024, fcae377, https://doi.org/10.1093/braincomms/fcae377. https://academic.oup.com/braincomms/article/6/6/fcae377/7845966. © The Author(s) 2024. Published by Oxford University Press on behalf of the Guarantors of Brain. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Recommended Citation
Nagy, Sara; Grange, Dorothy K; Sommerville, Richard; and et al., "Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations." Brain Communications. 6, 6. fcae377 (2024).
https://digitalcommons.wustl.edu/oa_4/7724
Department
ICTS (Institute of Clinical and Translational Sciences)
Additional Links
Supplemental material is available for this article at publisher site.
