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The Newcastle University research output collection, currently available on ePrints, will shortly be moving to a new open repository platform, Figshare. To prepare for the data migration we have paused adding new content to ePrints, and will resume once the new repository is launched. During this time you will continue to have access to ePrints (but no new content will appear). We will share updates here when available.

Case Report: Investigation and molecular genetic diagnosis of familial hypomagnesaemia: a case report

Lookup NU author(s): Dr Jamie Willows, Dr Noel Edwards, Dr Sarah RiceORCiD, Professor John SayerORCiD

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Licence

This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Publication metadata

Author(s): Willows J, Al Badi M, Richardson C, Al Sinani A, Edwards N, Rice SJ, Sayer JA

Publication type: Article

Publication status: Published

Journal: F1000Research

Year: 2019

Volume: 8

Online publication date: 15/05/2019

Acceptance date: 15/05/2019

Date deposited: 02/07/2019

ISSN (electronic): 2046-1402

Publisher: Faculty of 1000 Ltd

URL: https://doi.org/10.12688/f1000research.19006.2

DOI: 10.12688/f1000research.19006.2


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Funding

Funder referenceFunder name
BH160804

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