Gene mutation analysis in 12 Chinese children with congenital nephrotic syndrome

A Single-Gene Cause in 29.5% of Cases of Steroid-Resistant Nephrotic Syndrome

(2014) C. E. Sadowski et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Genotype–phenotype associations in WT1 glomerulopathy

(2014) Beata S. Lipska et al.   KIDNEY INTERNATIONAL

Laminin  2 Gene Missense Mutation Produces Endoplasmic Reticulum Stress in Podocytes

(2013) Y. M. Chen et al.   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

An Expanding Universe of FSGS Genes and Phenotypes: LMX1B Mutations Cause Familial Autosomal Dominant FSGS Lacking Extrarenal Manifestations

(2013) J. B. Kopp   JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY

Mutations in NPHS1 in a Chinese child with congenital nephrotic syndrome

(2012) Z.H. Yu et al.   GENETICS AND MOLECULAR RESEARCH

Mutation Analysis of NPHS1 in a Worldwide Cohort of Congenital Nephrotic Syndrome Patients

(2012) Bugsu Ovunc et al.   NEPHRON CLINICAL PRACTICE

Genetic Basis of Congenital and Infantile Nephrotic Syndromes

(2011) Joo Hoon Lee et al.   AMERICAN JOURNAL OF KIDNEY DISEASES

Clinical Utility of Genetic Testing in Children and Adults with Steroid-Resistant Nephrotic Syndrome

(2011) S. Santin et al.   Clinical Journal of the American Society of Nephrology

Two novel NPHS1 mutations in a Chinese family with congenital nephrotic syndrome

(2011) L.Q. Wu et al.   GENETICS AND MOLECULAR RESEARCH

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness

(2011) Saskia F. Heeringa et al.   JOURNAL OF CLINICAL INVESTIGATION

Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome

(2010) O. Boyer et al.   JOURNAL OF MEDICAL GENETICS

Nineteen novel NPHS1 mutations in a worldwide cohort of patients with congenital nephrotic syndrome (CNS)

(2010) Dominik S. Schoeb et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

Update on congenital nephrotic syndromes and the contribution of US

(2010) E. Fred Avni et al.   PEDIATRIC RADIOLOGY

WT1 Gene Mutations in Chinese Children With Early Onset Nephrotic Syndrome

(2010) Jianguo Li et al.   PEDIATRIC RESEARCH

The first Chinese Pierson syndrome with novel mutations in LAMB2

(2009) D. Zhao et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION

NPHS1 gene mutation in Japanese patients with congenital nephrotic syndrome

(2009) K. Aya et al.   NEPHROLOGY DIALYSIS TRANSPLANTATION