TUBB4B variants specifically impact ciliary function, causing a ciliopathic spectrum (2022)
Attributed to:
Congenital Anomalies - Patient-led Functional Genomics
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1101/2022.10.19.22280748
Publication URI: http://dx.doi.org/10.1101/2022.10.19.22280748
Type: Preprint