Cargando...
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...
Gardado en:
| Publicado en: | JIMD Rep |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Springer Berlin Heidelberg
2016
|
| Assuntos: | |
| Acceso en liña: | 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 |
| Tags: |
Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!
|