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Salla disease (SD) is a rare lysosomal storage disorder characterised by intellectual disability ataxia, athetosis, nystagmus, and central nervous system demyelination. Although the neurological spectrum of SD’s clinical phenotype is well defined,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2423::ef9eac1224fb66b532db903fba5f49f2
http://urn.fi/urn:nbn:fi-fe2022102763546
http://urn.fi/urn:nbn:fi-fe2022102763546