Nephropathic Cystinosis  >>  Phase N/A
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2 Trials

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Trial + Data / EventsStatusPhNRegionInterventionsSponsorConditionsPrimary complStudy compl
Nephropathic Cystinosis
NCT01995305: Use Massive Parallel Sequencing and Exome Capture Technology to Sequence the Exome of Fanconi Anemia Children and Their Patents

Available
N/A
RoW
human whole exome, whole genomic, whole exome
Xiaofan Zhu
Fanconi Anemia, Autosomal or Sex Linked Recessive Genetic Disease, Bone Marrow Hematopoiesis Failure, Multiple Congenital Abnormalities, and Susceptibility to Neoplastic Diseases., Hematopoiesis Maintainance.
 
 
CCIR, NCT01327807: Cure Cystinosis International Registry

Recruiting
N/A
750
US
Cystinosis Research Foundation
Cystinosis, Nephropathic Cystinosis, Renal Fanconi Syndrome
12/20
12/22

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