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Year | Number of Results |
---|---|
2002 | 2 |
2003 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 443954
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Abnormal glycosylation of red cell membrane band 3 in the congenital disorder of glycosylation Ig.
Pediatr Res. 2003 Aug;54(2):224-9. doi: 10.1203/01.PDR.0000072327.55955.F7. Epub 2003 May 7.
Pediatr Res. 2003.
PMID: 12736397
ALG12 mannosyltransferase defect in congenital disorder of glycosylation type lg.
Grubenmann CE, Frank CG, Kjaergaard S, Berger EG, Aebi M, Hennet T.
Grubenmann CE, et al.
Hum Mol Genet. 2002 Sep 15;11(19):2331-9. doi: 10.1093/hmg/11.19.2331.
Hum Mol Genet. 2002.
PMID: 12217961
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Congenital disorders of glycosylation type Ig is defined by a deficiency in dolichyl-P-mannose:Man7GlcNAc2-PP-dolichyl mannosyltransferase.
Chantret I, Dupré T, Delenda C, Bucher S, Dancourt J, Barnier A, Charollais A, Heron D, Bader-Meunier B, Danos O, Seta N, Durand G, Oriol R, Codogno P, Moore SE.
Chantret I, et al.
J Biol Chem. 2002 Jul 12;277(28):25815-22. doi: 10.1074/jbc.M203285200. Epub 2002 Apr 30.
J Biol Chem. 2002.
PMID: 11983712
Free article.
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