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	1.	Olmsted syndrome with erythromelalgia caused by recessive transient receptor potential vanilloid 3 mutations. [electronic resource] by Duchatelet, S Guibbal, L de Veer, S Fraitag, S Nitschké, P Zarhrate, M Bodemer, C Hovnanian, A Producer: 20150617 In: The British journal of dermatology vol. 171 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Allelic heterogeneity of SMARD1 at the IGHMBP2 locus. [electronic resource] by Maystadt, I Zarhrate, M Landrieu, P Boespflug-Tanguy, O Sukno, S Collignon, P Melki, J Verellen-Dumoulin, C Munnich, A Viollet, L Producer: 20040917 In: Human mutation vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36. [electronic resource] by Maystadt, I Zarhrate, M Leclair-Richard, D Estournet, B Barois, A Renault, F Routon, M-C Durand, M-C Lefebvre, S Munnich, A Verellen-Dumoulin, C Viollet, L Producer: 20060808 In: Neurology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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