Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure.

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Bibliographic Details
Title: Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure.
Authors: Esson, Gavin1, Logan, Ian1, Wood, Katrina2, Browning, Andrew C.3, Sayer, John A.1,4,5 john.sayer@newcastle.ac.uk
Source: Journal of Rare Diseases. 3/1/2024, Vol. 3 Issue 1, p1-8. 8p.
Database: Academic Search Ultimate
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ISSN:2731085X
DOI:10.1007/s44162-024-00031-4