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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2016
Materias:
Guidelines
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203850/
https://www.ncbi.nlm.nih.gov/pubmed/27671891
http://dx.doi.org/10.1007/s10545-016-9972-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5203850/
https://www.ncbi.nlm.nih.gov/pubmed/27671891
http://dx.doi.org/10.1007/s10545-016-9972-7

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