Methylmalonic acidemia caused by Homozygous Missense variant c.1837C>T in Exon 11 of the MMUT gene which is Variant of Uncertain Significance: A Case Report
G. Phani Kumar, Mashingbonio Dirinamai, B. Manishkumar, Susheel kumar saini, Ajay kumar saini, S. Kumari
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