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	21.	Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6. [electronic resource] by Hartmannová, Hana Piherová, Lenka Tauchmannová, Kateřina Kidd, Kendrah Acott, Philip D Crocker, John F S Oussedik, Youcef Mallet, Marcel Hodaňová, Kateřina Stránecký, Viktor Přistoupilová, Anna Barešová, Veronika Jedličková, Ivana Živná, Martina Sovová, Jana Hůlková, Helena Robins, Vicki Vrbacký, Marek Pecina, Petr Kaplanová, Vilma Houštěk, Josef Mráček, Tomáš Thibeault, Yves Bleyer, Anthony J Kmoch, Stanislav Producer: 20170720 In: Human molecular genetics vol. 25 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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