Title : Thirteen Patients with MAT1A Mutations Detected Through Newborn Screening: 13 Years' Experience.

Pub. Date : 2014

PMID : 24445979






1 Functional Relationships(s)
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1 CONCLUSION: These cases show that individuals with even single changes in the MAT1A gene may have elevations in methionine identified by newborn screening, which may persist for months after birth without any clinical consequences. Methionine methionine adenosyltransferase 1A Homo sapiens