Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations. (2024)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1093/braincomms/fcae377
PubMed Identifier: 39502942
Publication URI: http://europepmc.org/abstract/MED/39502942
Type: Journal Article/Review
Volume: 6
Parent Publication: Brain communications
Issue: 6
ISSN: 2632-1297