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Clinical Pediatrics

Impact Factor: 0.7 / 5-Year Impact Factor: 1.1

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Brief report

First published online 2020-10

Novel KLHL3 Variant in an Infant With Gordon Syndrome

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Volume 59, Issue 11

https://doi.org/10.1177/0009922820920938

Abstract

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References

1.

O’Shaughnessy

K

. Gordon syndrome: a continuing story. Pediatric Nephrol. 2014;30:1903-1908.

2.

Louis-Dit-Picard

H

Barc

J

Trujillano

D

, et al. KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron. Nat Genetics. 2012;44:456-460.

3.

Gereda

J

Bonilla-Felix

M

Kalil

B

Dewitt

S

. Neonatal presentation of Gordon syndrome. J Pediatr. 1996;129:615-661.

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