LMX1B Mutations Cause Hereditary FSGS without Extrarenal Involvement-Reference-Cited by-同舟云学术

LMX1B Mutations Cause Hereditary FSGS without Extrarenal Involvement

Published:2013-05-16 Issue:8 Volume:24 Page:1216-1222
ISSN:1046-6673
Container-title:Journal of the American Society of Nephrology
language:en
Short-container-title:JASN

Author:

Boyer Olivia,Woerner Stéphanie,Yang Fan,Oakeley Edward J.,Linghu Bolan,Gribouval Olivier,Tête Marie-Josèphe,Duca José S.,Klickstein Lloyd,Damask Amy J.,Szustakowski Joseph D.,Heibel Françoise,Matignon Marie,Baudouin Véronique,Chantrel François,Champigneulle Jacqueline,Martin Laurent,Nitschké Patrick,Gubler Marie-Claire,Johnson Keith J.,Chibout Salah-Dine,Antignac Corinne

Publisher

American Society of Nephrology (ASN)

Subject

Nephrology,General Medicine

Reference41 articles.

1. Pathologic classification of focal segmental glomerulosclerosis

2. Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

3. Donor splice-site mutations in WT1 are responsible for Frasier syndrome

4. Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome

5. Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis

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3. Identification of a novel LMX1B nonsense variant associated with congenital talipes equinovarus by prenatal exome sequencing: A case report;Molecular Genetics & Genomic Medicine;2023-11-06

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5. Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosis;Scientific Reports;2023-01-16