1034 a Hypotonic Infant With Methylene Tetrahydrofolate Reductase (MTHFR) Deficiency; Homozygous Mutation of C.1015T>G in MTFHR Gene
Archives of Disease in Childhood - United Kingdom
doi 10.1136/archdischild-2012-302724.1034
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Date
October 1, 2012
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BMJ