Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Susannah Boddie"'
Autor:
Emmanuelle Lecommandeur, Maria Begoña Cachón-González, Susannah Boddie, Ben D. McNally, Andrew W. Nicholls, Timothy M. Cox, Julian L. Griffin
Publikováno v:
Metabolites, Vol 11, Iss 1, p 18 (2020)
Sandhoff disease (SD) is a lysosomal disease caused by mutations in the gene coding for the β subunit of β-hexosaminidase, leading to deficiency in the enzymes β-hexosaminidase (HEX) A and B. SD is characterised by an accumulation of gangliosides
Externí odkaz:
https://doaj.org/article/2cfc0a9f51594020903d5a1919d93254
Autor:
Maria Begoña Cachón-González, Emmanuelle Lecommandeur, Ben D. McNally, Julian L. Griffin, Susannah Boddie, Andrew W. Nicholls, Timothy M. Cox
Publikováno v:
Metabolites; Volume 11; Issue 1; Pages: 18
Metabolites
Metabolites, Vol 11, Iss 18, p 18 (2021)
Metabolites
Metabolites, Vol 11, Iss 18, p 18 (2021)
Sandhoff disease (SD) is a lysosomal disease caused by mutations in the gene coding for the β subunit of β-hexosaminidase, leading to deficiency in the enzymes β-hexosaminidase (HEX) A and B. SD is characterised by an accumulation of gangliosides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d376916ace8ab6efdde0dfac6ce507ba
