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2004 | 1 |
2005 | 1 |
2024 | 0 |
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Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.
Am J Hum Genet. 2004 Jul;75(1):146-50. doi: 10.1086/422367. Epub 2004 May 17.
Am J Hum Genet. 2004.
PMID: 15148656
Free PMC article.
CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features.
Weinstein M, Schollen E, Matthijs G, Neupert C, Hennet T, Grubenmann CE, Frank CG, Aebi M, Clarke JT, Griffiths A, Seargeant L, Poplawski N.
Weinstein M, et al.
Am J Med Genet A. 2005 Jul 15;136(2):194-7. doi: 10.1002/ajmg.a.30851.
Am J Med Genet A. 2005.
PMID: 15945070
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