Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sophia R.L. Vieira"'
Publikováno v:
Movement Disorders. 35:1128-1133
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ae24eb7ddb19d0225d5ffb6c7591fed
https://doi.org/10.1002/mds.28030
https://doi.org/10.1002/mds.28030
Publikováno v:
Free radical biologymedicine. 175
Biallelic (homozygous or compound heterozygous) glucocerebrosidase gene (GBA) mutations cause Gaucher disease, whereas heterozygous mutations are numerically the most important genetic risk factor for Parkinson disease (PD) and are associated with th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58652c99868fe2255b02d541b3e92de1
https://pubmed.ncbi.nlm.nih.gov/34450264
https://pubmed.ncbi.nlm.nih.gov/34450264
Autor:
Sophia R.L. Vieira, Huw R. Morris
Publikováno v:
Frontiers in Neurology
Frontiers in Neurology, Vol 12 (2021)
Frontiers in Neurology, Vol 12 (2021)
Genetics has driven significant discoveries in the field of neurodegenerative diseases (NDDs). An emerging theme in neurodegeneration warrants an urgent and comprehensive update: that carrier status of early-onset autosomal recessive (AR) disease, ty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::807600cea742d3e7c2741c5b48ac6147
https://pubmed.ncbi.nlm.nih.gov/34149605
https://pubmed.ncbi.nlm.nih.gov/34149605