Modulation of Brain Cholesterol Metabolism through CYP46A1 Overexpression for Rett Syndrome

Modulation of Brain Cholesterol Metabolism through CYP46A1 Overexpression for Rett Syndrome

Rett syndrome (RTT) is a rare neurodevelopmental disorder caused by mutation in the X-linked gene methyl-CpG-binding protein 2 (Mecp2), a ubiquitously expressed transcriptional regulator. RTT results in mental retardation and developmental regression that affects approximately 1 in 10,000 females. C...

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Main Authors: Emilie Audouard (Author), Nicolas Khefif (Author), Béatrix Gillet-Legrand (Author), Fanny Nobilleau (Author), Ouafa Bouazizi (Author), Serena Stanga (Author), Gaëtan Despres (Author), Sandro Alves (Author), Antonin Lamazière (Author), Nathalie Cartier (Author), Françoise Piguet (Author)
Format: Book
Published: MDPI AG, 2024-06-01T00:00:00Z.
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3rd Floor Main Library

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