Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies
![Genes | Free Full-Text | Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis Genes | Free Full-Text | Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis](https://www.mdpi.com/genes/genes-12-00351/article_deploy/html/images/genes-12-00351-g001.png)
Genes | Free Full-Text | Sensory Reactivity Symptoms Are a Core Feature of ADNP Syndrome Irrespective of Autism Diagnosis
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Frontiers | ADNP, a Microtubule Interacting Protein, Provides Neuroprotection Through End Binding Proteins and Tau: An Amplifier Effect
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Frontiers | The Eight and a Half Year Journey of Undiagnosed AD: Gene Sequencing and Funding of Advanced Genetic Testing Has Led to Hope and New Beginnings
![Further evidence that a blepharophimosis syndrome phenotype is associated with a specific class of mutation in the ADNP gene - Takenouchi - 2017 - American Journal of Medical Genetics Part A - Wiley Online Library Further evidence that a blepharophimosis syndrome phenotype is associated with a specific class of mutation in the ADNP gene - Takenouchi - 2017 - American Journal of Medical Genetics Part A - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/d4d79869-5b96-428a-807d-dfe4d089c83e/ajmga38126-fig-0003-m.jpg)
Further evidence that a blepharophimosis syndrome phenotype is associated with a specific class of mutation in the ADNP gene - Takenouchi - 2017 - American Journal of Medical Genetics Part A - Wiley Online Library
![Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies - ScienceDirect Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0006322321016309-gr3.jpg)
Novel ADNP Syndrome Mice Reveal Dramatic Sex-Specific Peripheral Gene Expression With Brain Synaptic and Tau Pathologies - ScienceDirect
FONDAZIONE TELETHON - Camilla ha sette anni. Ed è affetta da una patologia genetica rara, la sindrome del gene ADNP. La famiglia ha ricevuto la diagnosi grazie al programma malattie rare di
![Early behavioral and developmental interventions in ADNP‐syndrome: A case report of SWI/SNF‐related neurodevelopmental syndrome - Shillington - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library Early behavioral and developmental interventions in ADNP‐syndrome: A case report of SWI/SNF‐related neurodevelopmental syndrome - Shillington - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/e37a1b6e-5cd2-4c83-9873-9466dc5a9218/mgg31230-fig-0001-m.jpg)
Early behavioral and developmental interventions in ADNP‐syndrome: A case report of SWI/SNF‐related neurodevelopmental syndrome - Shillington - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
![Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC](https://europepmc.org/articles/PMC6139063/bin/nihms-980073-f0005.jpg)
Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP. - Abstract - Europe PMC
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Genes | Free Full-Text | Helsmoortel–Van der Aa Syndrome—Cardiothoracic and Ectodermal Manifestations in Two Patients as Further Support of a Previous Observation on Phenotypic Overlap with RASopathies
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