Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure. (2024)
Attributed to:
Rare Disease Research Platform: The renal ciliopathies national network (RCNN)
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1007/s44162-024-00031-4
PubMed Identifier: 38433745
Publication URI: http://europepmc.org/abstract/MED/38433745
Type: Journal Article/Review
Volume: 3
Parent Publication: Journal of rare diseases (Berlin, Germany)
Issue: 1
ISSN: 2731-085X