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HLA-DR Patterns in Pernicious Anaemia. British Medical Journal (Clinical Research Ed.), vol

& Triantafyllou, K

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Cerebral folate deficiency in two siblings caused by biallelic variants including a novel mutation of FOLR1 gene: Intrafamilial heterogeneity following early treatment and the role of ketogenic diet

PGC-1 has multiple binding sites for the interactions with diverse coactivators
