Literature DB >> 11139267

A novel polymorphism (c288C>T) of the NPHS2 gene identified in a Taiwan Chinese family.

M C Wu1, J Y Wu, C C Lee, C H Tsai, F J Tsai.   

Abstract

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Year:  2001        PMID： 11139267     DOI： 10.1002/1098-1004(2001)17:1<81::AID-HUMU31>3.0.CO;2-U

Source DB:  PubMed          Journal:  Hum Mutat        ISSN： 1059-7794            Impact factor:   4.878


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  3 in total

1.  NPHS2 mutations in late-onset focal segmental glomerulosclerosis: R229Q is a common disease-associated allele.

Authors:  Hiroyasu Tsukaguchi; Akulapalli Sudhakar; Tu Cam Le; Trang Nguyen; Jun Yao; Joshua A Schwimmer; Asher D Schachter; Esteban Poch; Patricia F Abreu; Gerald B Appel; Aparecido B Pereira; Raghu Kalluri; Martin R Pollak
Journal:  J Clin Invest       Date:  2002-12       Impact factor: 14.808

2.  A novel mutation of NPHS2 identified in a Chinese family.

Authors:  Zihua Yu; Jie Ding; Na Guan; Yan Shi; Jingjing Zhang; Jianping Huang; Yong Yao; Jiyun Yang
Journal:  Pediatr Nephrol       Date:  2004-11       Impact factor: 3.714

3.  NPHS2 (podicin) mutations in Turkish children with idiopathic nephrotic syndrome.

Authors:  Afig Berdeli; Sevgi Mir; Onder Yavascan; Erkin Serdaroglu; Mustafa Bak; Nejat Aksu; Ayse Oner; Ali Anarat; Osman Donmez; Nurhan Yildiz; Lale Sever; Yilmaz Tabel; Ruhan Dusunsel; Ferah Sonmez; Nilgun Cakar
Journal:  Pediatr Nephrol       Date:  2007-09-25       Impact factor: 3.714
  3 in total

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