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Updated: Jan 27, 2026

Dissecting Cell-Autonomous Function of Fragile X Mental Retardation Protein in an Auditory Circuit by In Ovo Electroporation
Published on: July 6, 2022
Bain type of X-linked syndromic mental retardation in boys
Stefani Harmsen1, Rebecca Buchert2,3, Ertan Mayatepek1
1Department of General Pediatrics, Neonatology and Pediatric Cardiology, University Children's Hospital Duesseldorf, Medical Faculty, Heinrich Heine University, Duesseldorf, Germany.
Abstract:
A hemizygous variant in the HNRNPH2 gene causes MRXSB in a male individual.
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