Congenital nephrotic syndrome in an infant with ALG1 -congenital disorder of glycosylation-Reference-Cited by-同舟云学术

Congenital nephrotic syndrome in an infant with ALG1 -congenital disorder of glycosylation

Author:

Harshman Lyndsay A¹,Ng Bobby G²,Freeze Hudson H²,Trapane Pamela³,Dolezal Anna⁴,Brophy Patrick D¹,Brumbaugh Jane E⁵

Affiliation:

1. Division of Pediatric Nephrology, Stead Family Department of Pediatrics; University of Iowa Children's Hospital; Iowa City Iowa USA

2. Human Genetics Program Sanford Burnham Prebys Medical Discovery Institute; Sanford Children's Health Research Center; La Jolla CA USA

3. Division of Medical Genetics, Stead Family Department of Pediatrics; University of Iowa Children's Hospital; Iowa City Iowa USA

4. Department of Pathology; University of Iowa Carver College of Medicine; Iowa City Iowa USA

5. Division of Neonatology, Stead Family Department of Pediatrics; University of Iowa Children's Hospital; Iowa City Iowa USA

Funder

Rocket Fund and the National Institutes of Health

National Human Genome Research Institute and the National Heart, Lung and Blood Institute

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

Reference12 articles.

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