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An updated investigation on the dromedary camel cerebellum ( Camelus dromedarius ) with special insight into the distribution of calcium-binding proteins

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Ataxia‐telangiectasia (A‐T) is a rare genome instability and neurocutaneous syndrome caused by biallelic mutations in the ataxia‐telangiectasia mutated (ATM) gene, exhibiting an incidence of ~1:40,000–1:300,000 live births in different communities worldwide and a median survival rate of ~25 years (Collyer and Rajan 2024)