Methionine adenosyltransferase I/III deficiency: beyond the central ne | TCRM
Genes | Free Full-Text | Methionine Adenosyltransferase I/III Deficiency Detected by Newborn Screening
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Characterization of MAT I/III deficient patients' relatives | Download Scientific Diagram
Diagnostic Value of the MAT1A Gene Mutations in Methionine Adenosyltransferase I/III Deficiency: Possible Relevance to Various Neurological Manifestations
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Fructose-1,6-Diphosphatase Deficiency Misdiagnosed as Reye Syndrome - Enrico Zammarchi, Maria A. Donati, Federica Ciani, Pietro Rubetti, Elisabetta Pasquini, 1995
Methionine, AdoMet, and AdoHcy metabolism. AdoMet, S-... | Download Scientific Diagram
Frontiers | Long-term prognosis of 35 patients with methionine adenosyltransferase deficiency based on newborn screening in China
Hypermethioninemia: MedlinePlus Genetics
METHIONINE ADENOSYL-TRANSFERASE (MAT) DEFICIENCY
BKD (beta-ketothiolase deficiency) – newbornscreening.info
Methionine adenosyltransferases in cancers: Mechanisms of dysregulation and implications for therapy | Semantic Scholar
Methionine adenosyltransferase I/III deficiency: beyond the central nervous system manifestations
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Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders | Journal of Inherited Metabolic Disease
Methionine Adenosyltransferase - an overview | ScienceDirect Topics
Dominant inheritance of isolated hypermethioninemia is associated with a mutation in the human methionine adenosyltransferase 1A gene. - Abstract - Europe PMC
