Výsledky vyhľadávania
- A novel homozygous mutation in the human ALG12 gene results in an aberrant profile of oligomannose N-glycans in patient's serum / Ziburová J., Nemčovič M., Šesták S. ... [et al.] . American Journal of Medical Genetics Part A . - Vol. 185, no. 11 (2021), s. 3494-3501 [Dokument nie je vo fonde knižnice]
- Congenital disorders of glycosylation - an umbrella term for rapidly expanding group of rare genetic metabolic disorders - importance of physical investigation / Lekka D.E. ... [et al.] . Bratislavské lekárske listy : international journal for biomedical sciences and clinical medicine. - ISSN 0006-9248 . - Vol. 122, no. 3 (2021), s. 190-195 : ilustr., fareb. fotogr., schémy, tab.
- C 526