📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Ciliopathy patient variants reveal organelle-specific functions for TUBB4B in axonemal microtubules. (2024)

First Author: Dodd DO

Attributed to: Congenital Anomalies - Patient-led Functional Genomics funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1126/science.adf5489

PubMed Identifier: 38662826

Publication URI: http://europepmc.org/abstract/MED/38662826

Type: Journal Article/Review

Volume: 384

Parent Publication: Science (New York, N.Y.)

Issue: 6694

ISSN: 0036-8075