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Autor:
Aura, Tudor, Adriana, Muşat, Ana, Doscan, Maria, Bari, Carmen, Zapucioiu, Elena, Urdea, D, Cochior, D, Peţa
Publikováno v:
Romanian journal of internal medicine = Revue roumaine de medecine interne. 44(2)
Anderson Fabry disease (alpha galactosidase A deficiency) is an X-linked recessive lysosomal storage disorder; alpha galactosidase A deficiency results in accumulation of neutral glycosphingolipids, especially globotriaosylceramide (Gb3), in various
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f892b6d6f27cb843a3f1ba411649d260
https://pubmed.ncbi.nlm.nih.gov/17236300
https://pubmed.ncbi.nlm.nih.gov/17236300
