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	21.	Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. [electronic resource] by Brown, R M Head, R A Morris, A A M Raiman, J A J Walter, J H Whitehouse, W P Brown, G K Producer: 20060928 In: Developmental medicine and child neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Guanidinoacetate methyltransferase deficiency masquerading as a mitochondrial encephalopathy. [electronic resource] by Morris, A A M Appleton, R E Power, B Isherwood, D M Abernethy, L J Taylor, R W Turnbull, D M Verhoeven, N M Salomons, G S Jakobs, C Producer: 20070313 In: Journal of inherited metabolic disease vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	Homoplasmy, heteroplasmy, and mitochondrial dystonia. [electronic resource] by McFarland, R Chinnery, P F Blakely, E L Schaefer, A M Morris, A A M Foster, S M Tuppen, H A L Ramesh, V Dorman, P J Turnbull, D M Taylor, R W Producer: 20070928 In: Neurology vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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