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A fatty acid analogue targeting mitochondria exerts a plasma triacylglycerol lowering effect in rats with impaired carnitine biosynthesis

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Hypophosphatasia Autosomal dominant or autosomal recessive rare metabolic disease with an extraordinary range of severity caused by loss-of-function mutations within ALPL , which encodes TNALP

Cavadini P, Biasiotto G, Poli M et al (2007) RNA silencing of the mitochondrial ABCB7 transporter in HeLa cells causes an iron-deficient phenotype with mitochondrial iron overload