Common variations in ALG9 are not associated with bipolar I disorder: a family-based study

BACKGROUND: A mannosyltransferase gene (ALG9, DIBD1) at chromosome band 11q23 was previously identified to be disrupted by a balanced chromosomal translocation t(9;11)(p24;q23) co-segregating with bipolar affective disorder in a small family. Inborn ALG9 deficiency (congenital disorders of glycosyla...

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Autori principali: Baysal, Bora E, Willett-Brozick, Joan E, Bacanu, Silviu-Alin, Detera-Wadleigh, Sevilla, Nimgaonkar, Vishwajit L
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2006
Soggetti:
Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC1569366/
https://ncbi.nlm.nih.gov/pubmed/16859551
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1744-9081-2-25
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