Inherited glycosylphosphatidylinositol deficiency disorders: a new group of inherited metabolic disorders

Inherited glycosylphosphatidylinositol deficiency disorders (IGDs) are a group of rare congenital disorders of glycosylation with multisystemic involvement. The underlying cause is an abnormal structure of glycosylphosphatidylinositol, which plays a significant role in the attachment of proteins to...

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Bibliografiske detaljer

Principais autores:	Michał Patalan, Alicja Leśniak, Justyna Paprocka, Agnieszka Zubkiewicz-Kucharska, Kaja Giżewska-Kacprzak, Marta Glińska, Lidia Babiak-Choroszczak, Maria Giżewska, Robert Śmigiel
Format:	Artigo
Sprog:	Inglês
Udgivet:	Termedia Publishing House 2024-12-01
Serier:	Pediatria Polska
Fag:	congenital disorders of glycosylation inherited glycosylphosphatidylinositol deficiency disorders glycosylphosphatidylinositol-anchored proteins next-generation sequencing
Online adgang:	https://www.termedia.pl/Inherited-glycosylphosphatidylinositol-deficiency-disorders-a-new-group-of-inherited-metabolic-disorders,127,55419,1,1.html
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