DOI:
10.1055/s-00000041
Neuropediatrics
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References
Leclerc D, Campeau E, Goyette P. , et al.
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.
Hum Mol Genet 1996;
5 (12) 1867-1874
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