PubMed (OMIM) for id: 443955

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Year	Number of Results
1998	1
2002	1
2004	1
2023	0

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Page 1

Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.

Frank CG, Grubenmann CE, Eyaid W, Berger EG, Aebi M, Hennet T. Frank CG, et al. 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.

A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family.

Baysal BE, Willett-Brozick JE, Badner JA, Corona W, Ferrell RE, Nimgaonkar VL, Detera-Wadleigh SD. Baysal BE, et al. Neurogenetics. 2002 Mar;4(1):43-53. doi: 10.1007/s10048-001-0129-x. Neurogenetics. 2002. PMID: 12030331

Bipolar affective disorder partially cosegregates with a balanced t(9;11)(p24;q23.1) chromosomal translocation in a small pedigree.

Baysal BE, Potkin SG, Farr JE, Higgins MJ, Korcz J, Gollin SM, James MR, Evans GA, Richard CW 3rd. Baysal BE, et al. Am J Med Genet. 1998 Feb 7;81(1):81-91. Am J Med Genet. 1998. PMID: 9514593

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