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Publikováno v:
Neuroepidemiology.
Introduction: Huntington’s disease (HD) is a neurodegenerative, autosomal dominant disabling condition due to an expansion of the CAG trinucleotide in the HTT gene. Motor, psychiatric, and cognitive disorders characterize it. Chilean reports on HD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5461ac975adff92b5deacc5d34b94b7b
https://doi.org/10.1159/000528961
https://doi.org/10.1159/000528961
