Therapeutic Potential of αS Evolvability for Neuropathic Gaucher Disease

Gaucher disease (GD), the most common lysosomal storage disorder (LSD), is caused by autosomal recessive mutations of the glucocerebrosidase gene, GBA1. In the majority of cases, GD has a non-neuropathic chronic form with adult onset (GD1), while other cases are more acute and severer neuropathic fo...

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Detalles Bibliográficos
Autores principales: Wei, Jianshe, Takamatsu, Yoshiki, Wada, Ryoko, Fujita, Masayo, Ho, Gilbert, Masliah, Eliezer, Hashimoto, Makoto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Perspective
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919466/
https://www.ncbi.nlm.nih.gov/pubmed/33672048
http://dx.doi.org/10.3390/biom11020289

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7919466/
https://www.ncbi.nlm.nih.gov/pubmed/33672048
http://dx.doi.org/10.3390/biom11020289

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