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General Physiology 151 (10), 12311246

Uchida, H., Nakajima, Y., Ohtake, K., Ito, J., Morita, M., Kamimura, A., & Kobayashi, J

Methylmalonic Aciduria and Homocystinuria, cblF Type|MAHCF an autosomal recessive form of combined methylmalonic aciduria and homocystinuria, caused by mutation(s) in the abcd4 gene, encoding lysosomal cobalamin transporter abcd4

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