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There is a page named "SRD5A3-CDG" on Wikipedia
- SRD5A3-CDG (also known as CDG syndrome type Iq, CDG-Iq, CDG1Q or Congenital disorder of glycosylation type 1q) is a rare, non X-linked congenital disorder...11 KB (1,321 words) - 05:05, 1 December 2023
- an enzyme that in humans is encoded by the SRD5A3 gene. It is one of three forms of 5α-reductase. SRD5A3-CDG Congenital disorder of glycosylation Kahrizi...2 KB (314 words) - 05:45, 17 June 2024
- Congenital disorder of glycosylation (redirect from CDG syndrome)common finding. Some CDG subtypes, like SSR4-CDG 1y, have been classified as connective tissue disorders. Ocular abnormalities of PMM2-CDG include: myopia...41 KB (3,740 words) - 23:31, 13 August 2024
- transport function. SRD5A3-CDG PMM2 deficiency "SLC35A1-CDG (CDG-IIf)". RESERVADOS, INSERM US14-- TODOS LOS DERECHOS. "Orphanet: SLC35A1 CDG". www.orpha.net...14 KB (1,432 words) - 15:08, 27 October 2023