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Autor:
Irina Zh. Zhalsanova, Ekatherina G. Ravzhaeva, Anna E. Postrigan, Gulnara N. Seitova, Daria I. Zhigalina, Vasilisa Yu. Udalova, Maryana M. Danina, Ilya V. Kanivets, Nikolay A. Skryabin
Publikováno v:
International Journal of Molecular Sciences. 23:10606
Rafiq syndrome (RAFQS) is a congenital disorder of glycosylation (CDG) that is caused by mutations in the MAN1B1 gene and characterized by impaired protein and lipid glycosylation. RAFQS is characterized by a delay in intellectual and motor developme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b8d9bfe3a49b913fe2b512eea92d1d2
https://doi.org/10.3390/ijms231810606
https://doi.org/10.3390/ijms231810606
