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Scope of report The report provides brief overview of Preclinical RA. This report discusses ‘risk factors for development of RA’ and ‘at risk population’. This report provides comparison of ‘at risk population’ and ‘classified RA patients’ based on biomarker analysis. This report discusses lessons learned from animal studies This report elaborates biomarker insight from retrospective human studies The report covers clinical therapeutics in development for preclinical RA including product profiles, trial summaries. The report mentions

Rett syndrome (RTT) is a rare neuro-developmental disorder (incidence: approximately one out of 10,000 female births) that reached worldwide prominence in the early 1980s. Owing to its predominance in females, Rett syndrome is regarded as a genetic disorder. Over the past 25 years, understanding of the clinical features and natural history of this unique neuro-developmental disorder has evolved dramatically. Significant advances have emerged in recent years regarding our understanding of the clinical features, molecular genetics

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