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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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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2006
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| Assuntos: | |
| Acesso em linha: | 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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