Article info
PostScript
Letter
Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia
- Correspondence to Dr Fahmi Nasrallah, Rabta Hospital, Tunis 1007, Tunisia; fehmi56{at}yahoo.fr
Citation
Non-ketotic hyperglycinaemia: a frequent, but poorly diagnosed and managed genetic disorder in Tunisia
Publication history
- Accepted April 23, 2020
- First published May 13, 2020.
Online issue publication
January 08, 2022
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- Previous version (19 February 2021).
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© Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.