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	101.	MeCP2 mutations in children with and without the phenotype of Rett syndrome. [electronic resource] by Hoffbuhr, K Devaney, J M LaFleur, B Sirianni, N Scacheri, C Giron, J Schuette, J Innis, J Marino, M Philippart, M Narayanan, V Umansky, R Kronn, D Hoffman, E P Naidu, S Producer: 20010712 In: Neurology vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	102.	Genotype-phenotype correlation in vanishing white matter disease. [electronic resource] by van der Lei, H D W van Berkel, C G M van Wieringen, W N Brenner, C Feigenbaum, A Mercimek-Mahmutoglu, S Philippart, M Tatli, B Wassmer, E Scheper, G C van der Knaap, M S Producer: 20101112 In: Neurology vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	103.	Mutations in the palmitoyl-protein thioesterase gene (PPT; CLN1) causing juvenile neuronal ceroid lipofuscinosis with granular osmiophilic deposits. [electronic resource] by Mitchison, H M Hofmann, S L Becerra, C H Munroe, P B Lake, B D Crow, Y J Stephenson, J B Williams, R E Hofman, I L Taschner, P E Martin, J J Philippart, M Andermann, E Andermann, F Mole, S E Gardiner, R M O'Rawe, A M Producer: 19980317 In: Human molecular genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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