Posterior Cranial Fossa Malformation and Vascular Dysplasia in GJB2 Gene Mutation-Reference-Cited by-同舟云学术

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Posterior Cranial Fossa Malformation and Vascular Dysplasia in GJB2 Gene Mutation

Published:2023-09-08 Issue: Volume: Page:1-3
ISSN:0317-1671
Container-title:Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques
language:en
Short-container-title:Can. J. Neurol. Sci.

Author:

Cesaroni Carlo Alberto^ORCID,Napoli Manuela,Spagnoli Carlotta^ORCID,Rizzi Susanna,Frattini Daniele,Fusco Carlo

Publisher

Cambridge University Press (CUP)

Subject

Neurology (clinical),Neurology,General Medicine

Reference8 articles.

1. Genetics landscape of nonsyndromic hearing loss in Indian populations;Ray;J Pediatr Genet,2021

2. Focal Adhesion Kinase Modulates Radial Glia-Dependent Neuronal Migration through Connexin-26

3. Connexin-26-Mutation bei "Keratitis-Ichthyosis-Deafness"-Syndrom (KID-Syndrom). Connexin 26 mutation and keratitis-ichthyosis-deafness (KID) Syndrome

4. Pathological mechanisms of connexin26-related hearing loss: Potassium recycling, ATP-calcium signaling, or energy supply?

5. Congenital Malformations of Cerebellum

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