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Autosomal recessive cerebellar ataxia with spasticity due to a rare mutation in GBA2 gene in a large consanguineous Saudi family

The nonlysosomal glucosylceramidase β2 (GBA2) gene encode an enzyme that catalyzes the hydrolysis of glucosylceramide to glucose and ceramide. Mutations in the GBA2 gene have been reported to cause hereditary spastic paraplegia, autosomal recessive cerebellar ataxia with spasticity, and Marinescu-Sj...

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Détails bibliographiques
Publié dans:Genes Dis
Auteurs principaux: Algahtani, Hussein, Shirah, Bader, Ullah, Ikram, Al-Qahtani, Mohammad H., Abdulkareem, Angham Abdulrahman, Naseer, Muhammad Imran
Format: Artigo
Langue:Inglês
Publié: Chongqing Medical University 2019
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC7859417/
https://ncbi.nlm.nih.gov/pubmed/33569519
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2019.07.009
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