Akademik Veri Yönetim Sistemi
CLINICAL JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, cilt.12, sa.10, ss.1634-1641, 2017 (SCI-Expanded)
Background and objectives Infantile nephropathic cystinosis is a severe disease that occurs due to mutations in the cystinosis gene, and it is characterized by progressive dysfunction of multiple organs; >100 cystinosis gene mutations have been identified in multiple populations. Our study aimed to identify the clinical characteristics and spectrum of cystinosis gene mutations in Turkish pediatric patients with cystinosis.