Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Chernin, Gil; Vega-Warner, Virginia; Schoeb, Dominik; Heeringa, Saskia; Ovunc, Bugsu; Saisawat, Pawaree; Cleper, Roxana; ÖZALTIN, FATİH; Hildebrandt, Friedhelm

doi:10.2215/cjn.09351209

Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations

Atıf İçin Kopyala

Chernin G., Vega-Warner V., Schoeb D. S., Heeringa S. F., Ovunc B., Saisawat P., ...Daha Fazla

CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.5, sa.9, ss.1655-1662, 2010 (SCI-Expanded)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 5 Sayı: 9
Basım Tarihi: 2010
Doi Numarası: 10.2215/cjn.09351209
Dergi Adı: CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.1655-1662
Hacettepe Üniversitesi Adresli: Evet

Özet

Background and objectives: The risk of developing Wilms tumor (WT) can be present or absent in patients with nephrotic syndrome (NS) caused by WT1 mutations. Here, the genotype/phenotype correlation regarding the outcome and risk for WT in 52 patients from 51 families with NS due to WT1 mutations is described.