GGDB-2020

Documents (337) JSON TSV

source DB	source ID	text	size	updated at	# proj.	# Ann.	updated_at
PubMed	10359825	A mutation in the human ortholog of the Saccharomyces cerevisiae ALG6 gene causes carbohydrate-defic	1.71 KB	2018-12-10	8	9	2021-12-17
PubMed	10536037	Cloning and expression of a human gene encoding an N-acetylgalactosamine-alpha2,6-sialyltransferase	1.85 KB	2019-05-30	64	6	2021-12-17
PubMed	10639137	The putative tumor suppressors EXT1 and EXT2 form a stable complex that accumulates in the Golgi app	1.31 KB	2015-11-15	9	17	2021-12-17
PubMed	11115853	Neuronal expression of the fukutin gene. Fukuyama-type congenital muscular dystrophy (FCMD), a relat	1.74 KB	2015-11-17	6	15	2021-12-17
PubMed	11592034	Mutations in the fukutin-related protein gene (FKRP) cause a form of congenital muscular dystrophy w	1.91 KB	2015-11-17	13	13	2021-12-17
PubMed	11741828	Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a	1.84 KB	2015-11-17	6	16	2021-12-17
PubMed	10187838	Molecular cloning and characterization of a human uronyl 2-sulfotransferase that sulfates iduronyl a	1.71 KB	2015-11-17	42	1	2021-12-17
PubMed	11326279	The gene defective in leukocyte adhesion deficiency II encodes a putative GDP-fucose transporter. Le	1.54 KB	2015-11-17	5	2	2021-12-17
PubMed	11326280	Complementation cloning identifies CDG-IIc, a new type of congenital disorders of glycosylation, as	1.76 KB	2015-11-17	5	6	2021-12-17
PubMed	11983712	Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7G	1.57 KB	2015-11-17	28	1	2021-12-17