DYNC2H1 hypomorphic or retina-predominant variants cause nonsyndromic retinal degeneration. (2020)

First Author: Vig A
Attributed to:  Dissecting the Molecular Mechanism of Intraflagellar Transport Motors funded by BBSRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1038/s41436-020-0915-1

PubMed Identifier: 32753734

Publication URI: http://europepmc.org/abstract/MED/32753734

Type: Journal Article/Review

Volume: 22

Parent Publication: Genetics in medicine : official journal of the American College of Medical Genetics

Issue: 12

ISSN: 1098-3600