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Article

CTNS Mutations in an American-Based Population of Cystinosis Patients

1 Nov 1998

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Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9792862
DOI: 10.1086/302118

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

CTNS Mutations in an American-Based Population of Cystinosis PatientsPMID 9792862Read ↗

Genetic analysis of two Iranian patients affected with cystinosis identified a novel CTNS mutation: case reportSemantic proximity Read ↗

Genetic basis of cystinosis in Turkish patients: a single-center experience.Semantic proximity Read ↗

CTNS mutations in patients with cystinosis.Semantic proximity Read ↗

Characterization of CTNS mutations in Arab patients with cystinosis.Semantic proximity Read ↗

Uncovering the Prevalence of Cystinosis through Genetic AnalysisSemantic proximity Read ↗

Molecular Basis of Cystinosis: Geographic Distribution, Functional Consequences of Mutations in the CTNS Gene, and Potential for RepairSemantic proximity Read ↗

Molecular characterization of cystinosis patients: predominance of the CTNS c.829dup mutation in Center of Tunisia.Semantic proximity Read ↗

Molecular Characterization of Tunisian Cystinosis Patients Reveals a High Prevalence of the c.829dup MutationSemantic proximity Read ↗

CTNS molecular genetics profile in a Persian nephropathic cystinosis population.Semantic proximity Read ↗

Identification of 14 novelCTNS mutations and characterization of seven splice site mutations associated with cystinosisSemantic proximity Read ↗

CTNS mutations in African American patients with cystinosis.Semantic proximity Read ↗

Phenotypic variability in cystinosis: Lessons from an atypical case.Semantic proximity Read ↗

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