Mutations in alpha-B-crystallin cause autosomal dominant axonal Charcot-Marie-Tooth disease with congenital cataracts. (2024)
Abstract
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Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1111/ene.16063
PubMed Identifier: 37772343
Publication URI: http://europepmc.org/abstract/MED/37772343
Type: Journal Article/Review
Volume: 31
Parent Publication: European journal of neurology
Issue: 1
ISSN: 1351-5101