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Description
Homocystinuria-Megaloblastic Anemia, cblE Complementation Type|HMAE|Methylcobalamin Deficiency, cblE Type methylmalonic aciduria and homocystinuria type d protein, mitochondrial (296 aa, ~33 kda) is encoded by the human mmadhc gene
Apolipoprotein J: A new predictor and therapeutic target in cardiovascular disease
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A research guide to mechanism, the documented decline with ageing, and laboratory applications
