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Glycine N-Methyltransferase Deficiency: A Member of Dysmethylating Liver Disorders?
Glycine N-methyltransferase deficiency is an inherited disorder of methionine metabolism, reported so far in only four patients and characterised by permanent hypermethioninemia. This disorder has been considered as probably benign because moderate hepatomegaly in two patients was the only obvious s...
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| Publicado no: | JIMD Rep |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5388635/ https://ncbi.nlm.nih.gov/pubmed/27207470 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/8904_2016_543 |
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