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Japanese Journal of Clinical Immunology, ISSN 0911-4300, 07/2015, Volume 38, Issue 3, pp. 142 - 149
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Clinical immunology (Orlando, Fla.), 09/2019, pp. 108256 - 108256
Hereditary folate malabsorption (HFM) is an autosomal recessive disease caused by mutations in SLC46A1 encoding the proton-coupled folate transporter (PCFT).... 
Index Medicus
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