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New murine Niemann-Pick type C models bearing a pseudoexon-generating mutation recapitulate the main neurobehavioural and molecular features of the disease | Scientific Reports
Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive | Journal of Medical Genetics
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Figures and data in Inducible and reversible phenotypes in a novel mouse model of Friedreich's Ataxia | eLife