NAD deficiency, congenital malformations, and niacin supplementation
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109897.pdf. |
Description
Background Congenital malformations can be manifested as combinations of phenotypes that co-occur more often than expected by chance. In many such cases, it has proved difficult to identify a genetic cause. We sought the genetic cause of cardiac, vertebral, and renal defects, among others, in unrelated patients...
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| ID Code: | 109897 | ||||||||
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| Item Type: | Contribution to Journal (Journal Article) | ||||||||
| Refereed: | Yes | ||||||||
| ORCID iD: |
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| Measurements or Duration: | 9 pages | ||||||||
| DOI: | 10.1056/NEJMoa1616361 | ||||||||
| ISSN: | 1533-4406 | ||||||||
| Pure ID: | 33234947 | ||||||||
| Divisions: | Past > QUT Faculties & Divisions > Faculty of Health Past > Institutes > Institute of Health and Biomedical Innovation Current > Schools > School of Biomedical Sciences |
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| Copyright Owner: | Consult author(s) regarding copyright matters | ||||||||
| Copyright Statement: | This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the document is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recognise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to qut.copyright@qut.edu.au | ||||||||
| Deposited On: | 22 Aug 2017 05:11 | ||||||||
| Last Modified: | 08 Aug 2024 09:17 |
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