Molecular Pathogenic Mechanisms of Hypomyelinating Leukodystrophies (HLDs)

Hypomyelinating leukodystrophies (HLDs) represent a group of congenital rare diseases for which the responsible genes have been identified in recent studies. In this review, we briefly describe the genetic/molecular mechanisms underlying the pathogenesis of HLD and the normal cellular functions of t...

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Detalles Bibliográficos
Autores principales: Torii, Tomohiro, Yamauchi, Junji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538087/
https://www.ncbi.nlm.nih.gov/pubmed/37755363
http://dx.doi.org/10.3390/neurolint15030072

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10538087/
https://www.ncbi.nlm.nih.gov/pubmed/37755363
http://dx.doi.org/10.3390/neurolint15030072

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