Variants in <i>AQP11</i> may result in autosomal recessive bilateral cystic renal dysgenesis-Reference-Cited by-同舟云学术

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Variants in AQP11 may result in autosomal recessive bilateral cystic renal dysgenesis

Published:2022-11-24 Issue:2 Volume:191 Page:612-616
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:American J of Med Genetics Pt A

Author:

Price Michael E.¹,Fishler Kristen P.²,Muff‐Luett Melissa³,Mauch Teri J.³⁴,Brunelli Luca³⁴,Euteneuer Joshua C.³^ORCID

Affiliation:

1. University of Nebraska Medical Center, College of Medicine Omaha Nebraska USA

2. Munroe‐Meyer Institute of Genetics and Rehabilitation University of Nebraska Medical Center Omaha Nebraska USA

3. Department of Pediatrics University of Nebraska Medical Center Omaha Nebraska USA

4. Department of Pediatrics University of Utah Salt Lake City Utah USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.63056

Reference23 articles.

1. Human aquaporin-11 guarantees efficient transport of H2O2 across the endoplasmic reticulum membrane

2. Genetics of Congenital Anomalies of the Kidney and Urinary Tract: The Current State of Play

3. Aquaporin 11 variant associates with kidney disease in type 2 diabetic patients

4. Diagnostic Utility of Exome Sequencing for Kidney Disease

5. Aquaporin 11 rs2276415 variant and progression of chronic kidney disease

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