Focal segmental glomerulosclerosis in patients with complete deletion of one WT1 allele

Pediatrics

Volumn 129, Issue 6, 2012, Pages

  Iijima, Kazumoto ^a   Someya, Tomonosuke ^b   Ito, Shuichi ^c   Nozu, Kandai ^a   Nakanishi, Koichi ^c   Matsuoka, Kentaro ^d   Ohashi, Hirofumi ^e   Nagata, Michio ^f   Kamei, Koichi ^c   Sasaki, Satoshi ^g  

^a KOBE UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b JUNTENDO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c NATIONAL CENTER FOR CHILD HEALTH AND DEVELOPMENT   (Japan)

^d WAKAYAMA MEDICAL UNIVERSITY   (Japan)

^e SAITAMA CHILDREN'S MEDICAL CENTER   (Japan)

^f UNIVERSITY OF TSUKUBA   (Japan)

^g HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

Author keywords

Deletion; Focal segmental glomerulosclerosis; WAGR syndrome; WT1

Indexed keywords

CREATININE; DIPEPTIDYL CARBOXYPEPTIDASE INHIBITOR; PROTEIN; WT1 PROTEIN;

ALLELE; ANIRIDIA; ARTICLE; CANCER CHEMOTHERAPY; CANCER RADIOTHERAPY; CASE REPORT; CHILD; CHROMOSOME DELETION; CREATININE URINE LEVEL; CRYPTORCHISM; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; FOCAL GLOMERULOSCLEROSIS; GENE; GENE DELETION; HAPLOINSUFFICIENCY; HISTOLOGY; HUMAN; HUMAN TISSUE; HYPOSPADIAS; KIDNEY BIOPSY; KIDNEY FUNCTION; MALE; MENTAL DEFICIENCY; MICROALBUMINURIA; MICROPHTHALMIA; NEPHRECTOMY; NEPHROBLASTOMA; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; PROTEIN URINE LEVEL; PROTEINURIA; RENAL PROTECTION; UROGENITAL TRACT DISEASE; VESICOURETERAL REFLUX; WT1 GENE;

ADOLESCENT; ADULT; ALLELES; CHILD; CHILD, PRESCHOOL; FEMALE; GENE DELETION; GENES, DOMINANT; GLOMERULOSCLEROSIS, FOCAL SEGMENTAL; HUMANS; MALE; MUTATION, MISSENSE; WT1 PROTEINS;

EID: 84861902651     PISSN: 00314005     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.2011-1323     Document Type: Article

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