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Article

The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1

15 Feb 2014

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 24534056
DOI: 10.1016/j.braindev.2014.01.010

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The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1PMID 24534056Read ↗

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