A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan-Reference-Cited by-同舟云学术

A spectrum of novel NPHS1 and NPHS2 gene mutations in pediatric nephrotic syndrome patients from Pakistan

Published:2012-07 Issue:2 Volume:502 Page:133-137
ISSN:0378-1119
Container-title:Gene
language:en
Short-container-title:Gene

Author:

Abid Aiysha,Khaliq Shagufta,Shahid Saba,Lanewala Ali,Mubarak Mohammad,Hashmi Seema,Kazi Javed,Masood Tahir,Hafeez Farkhanda,Naqvi Syed Ali Anwar,Rizvi Syed Adeebul Hasan,Mehdi Syed Qasim

Publisher

Elsevier BV

Subject

Genetics,General Medicine

Reference34 articles.

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2. Update on congenital nephrotic syndromes and the contribution of US;Avni;Pediatr. Radiol.,2011

3. Analysis of recessive CD2AP and ACTN4 mutations in steroid-resistant nephrotic syndrome;Benoit;Pediatr. Nephrol.,2010

4. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome;Boute;Nat. Genet.,2000

5. Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome;Boyer;J. Med. Genet.,2010

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