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Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.

Systematic review · J Inherit Metab Dis · 2015. Source record refreshed; an explanation has not been reviewed.

Systematic reviewSource: PubMed · PMID 25762406

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Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.

Huemer M, Kožich V, Rinaldo P et al.
J Inherit Metab Dis · 2015

PubMed ID
25762406
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