Cortical interneuron development is affected in 4H leukodystrophy

4H leukodystrophy is a rare genetic disorder classically characterized by hypomyelination, hypodontia and hypogonadotropic hypogonadism. With the discovery that 4H is caused by mutations that affect RNA polymerase III, mainly involved in the transcription of small non-coding RNAs, patients with atyp...

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Detalles Bibliográficos
Autores principales: Dooves, Stephanie, Kok, Liza M L, Holmes, Dwayne B, Breeuwsma, Nicole, Breur, Marjolein, Bugiani, Marianna, Wolf, Nicole I, Heine, Vivi M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316783/
https://www.ncbi.nlm.nih.gov/pubmed/36729681
http://dx.doi.org/10.1093/brain/awad017

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316783/
https://www.ncbi.nlm.nih.gov/pubmed/36729681
http://dx.doi.org/10.1093/brain/awad017

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