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Exome sequencing identifies a likely causative variant in 53% of families with ciliopathy-related features on renal ultrasound after excluding NPHP1 deletions

Details

Language :
English
ISSN :
23523042
Volume :
11
Issue :
5
Database :
Directory of Open Access Journals
Journal :
Genes and Diseases
Publication Type :
Academic Journal
Accession number :
edsdoj.9dbf15b34e7843c2a166f0460ac001f4
Document Type :
article
Full Text :
https://doi.org/10.1016/j.gendis.2023.101111