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

Pediatric Nephrology

Volumn 22, Issue 12, 2007, Pages 2031-2040

  Berdeli, Afig ^a   Mir, Sevgi ^a   Yavascan, Onder ^a   Serdaroglu, Erkin ^b   Bak, Mustafa ^b   Aksu, Nejat ^c   Oner, Ayse ^d   Anarat, Ali ^e   Donmez, Osman ^f   Yildiz, Nurhan ^g   Sever, Lale ^h   Tabel, Yilmaz ⁱ   Dusunsel, Ruhan ^j   Sonmez, Ferah ^k   Cakar, Nilgun ^l  

^a EGE UNIVERSITY   (Turkey)

^b Behcet Uz Children's Hospital   (Turkey)

^c Tepecik Teaching and Research Hospital   (Turkey)

^d DR SAMI ULUS CHILDREN S HOSPITAL   (Turkey)

^e CUKUROVA UNIVERSITY   (Turkey)

^f ULUDAG UNIVERSITY   (Turkey)

^g Goztepe Teaching and Research Hospital ^*  (Turkey)

^h ISTANBUL UNIVERSITY   (Turkey)

ⁱ INONU UNIVERSITY   (Turkey)

^j ERCIYES UNIVERSITY   (Turkey)

^k ADNAN MENDERES UNIVERSITY   (Turkey)

^l Diskapi Education and Research Hospital   (Turkey)

more..

Author keywords

Children; Focal segmental glomerulosclerosis (FSGS); Nephrotic syndrome; Podocin mutation

Indexed keywords

CYCLOPHOSPHAMIDE; CYCLOSPORIN A; PODOCIN; PREDNISOLONE; STEROID;

ARTICLE; CHILD; CHILD HEALTH; CONTROLLED STUDY; DNA SEQUENCE; EXON; FEMALE; GENE MUTATION; GENETIC RISK; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; HUMAN TISSUE; KIDNEY FAILURE; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NEPHROTIC SYNDROME; ONSET AGE; POPULATION GENETICS; PRIORITY JOURNAL; PROGNOSIS; RISK FACTOR; TURKEY (REPUBLIC);

ADOLESCENT; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; INFANT; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; KIDNEY; KIDNEY FAILURE, CHRONIC; MALE; MEMBRANE PROTEINS; MUTATION; NEPHROTIC SYNDROME; TURKEY;

EID: 36048978116     PISSN: 0931041X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00467-007-0595-y     Document Type: Article

References (36)

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