New Approaches to Tay-Sachs Disease Therapy

Tay-Sachs disease belongs to the group of autosomal-recessive lysosomal storage metabolic disorders. This disease is caused by β-hexosaminidase A (HexA) enzyme deficiency due to various mutations in α-subunit gene of this enzyme, resulting in GM2 ganglioside accumulation predominantly in lysosomes o...

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Bibliografiska uppgifter
I publikationen:Front Physiol
Huvudupphovsmän: Solovyeva, Valeriya V., Shaimardanova, Alisa A., Chulpanova, Daria S., Kitaeva, Kristina V., Chakrabarti, Lisa, Rizvanov, Albert A.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Frontiers Media S.A. 2018
Ämnen:
Physiology
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC6256099/
https://ncbi.nlm.nih.gov/pubmed/30524313
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2018.01663
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