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Autosomal recessive VWA1-related disorder: comprehensive analysis of phenotypic variability and genetic mutations. (2024)

First Author: Nagy S

Attributed to: Identifying New Disease Genes & Mechanisms for Musculoskeletal Disorders in 100K Genomes Project using Bioinformatics, Phenotyping & Machine Learning funded by MRC

Abstract

No abstract provided

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