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

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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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  Data: Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure.
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  Data: <searchLink fieldCode="AR" term="%22Esson%2C+Gavin%22">Esson, Gavin</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Logan%2C+Ian%22">Logan, Ian</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Wood%2C+Katrina%22">Wood, Katrina</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Browning%2C+Andrew+C%2E%22">Browning, Andrew C.</searchLink><relatesTo>3</relatesTo><br /><searchLink fieldCode="AR" term="%22Sayer%2C+John+A%2E%22">Sayer, John A.</searchLink><relatesTo>1,4,5</relatesTo><i> john.sayer@newcastle.ac.uk</i>
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  Data: <searchLink fieldCode="JN" term="%22Journal+of+Rare+Diseases%22">Journal of Rare Diseases</searchLink>. 3/1/2024, Vol. 3 Issue 1, p1-8. 8p.
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        Value: 10.1007/s44162-024-00031-4
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        Text: English
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      – TitleFull: Diverse retinal-kidney phenotypes associated with NPHP1 homozygous whole-gene deletions in patients with kidney failure.
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            NameFull: Esson, Gavin
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            NameFull: Wood, Katrina
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              Text: 3/1/2024
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              Y: 2024
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