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RAN gene

Discuss publications and research concerning the RAN gene.

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Related literature

Variable Phenotype in Three Siblings With RAN Binding Protein 2 Variant With Potential Preventive Treatment for Recurrences.
RAN
Polymorphic CGG repeats in gene regulation and disease.
RAN
Single nucleotide polymorphisms of GEMIN3 modify the risk of primary Sjögren's syndrome in female patients.
RAN
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
RAN
Repeat-Associated Non-ATG Translation in Neurological Diseases.
RAN
[Recent Topics in Autosomal Dominantly Inherited Spinocerebellar Ataxias].
RAN
Understanding decreased fertility in women carriers of the FMR1 premutation: a possible mechanism for Fragile X-Associated Primary Ovarian Insufficiency (FXPOI).
RAN
Beyond loss of frataxin: the complex molecular pathology of Friedreich ataxia.
RAN
Unconventional translation of C9ORF72 GGGGCC expansion generates insoluble polypeptides specific to c9FTD/ALS.
RAN
Outcomes of empirical eating disorder phenotypes in a clinical female sample: results from a latent class analysis.
RAN

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