Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders

Inherited methylation disorders are a group of rarely reported, probably largely underdiagnosed disorders affecting transmethylation processes in the metabolic pathway between methionine and homocysteine. These are methionine adenosyltransferase I/III, glycine N-methyltransferase, S-adenosylhomocyst...

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Detalhes bibliográficos
Publicado no:J Inherit Metab Dis
Main Authors: Barić, Ivo, Staufner, Christian, Augoustides-Savvopoulou, Persephone, Chien, Yin-Hsiu, Dobbelaere, Dries, Grünert, Sarah C., Opladen, Thomas, Petković Ramadža, Danijela, Rakić, Bojana, Wedell, Anna, Blom, Henk J.
Formato: Artigo
Idioma:Inglês
Publicado em: Springer Netherlands 2016
Assuntos:
Guidelines
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5203850/
https://ncbi.nlm.nih.gov/pubmed/27671891
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10545-016-9972-7
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