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	1.	Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions in ATP7A. [electronic resource] by Tümer, Zeynep Birk Møller, Lisbeth Horn, Nina Producer: 20040126 In: Human mutation vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Structural models of the human copper P-type ATPases ATP7A and ATP7B. [electronic resource] by Gourdon, Pontus Sitsel, Oleg Lykkegaard Karlsen, Jesper Birk Møller, Lisbeth Nissen, Poul Producer: 20121212 In: Biological chemistry vol. 393 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Characterization of ATP7A missense mutants suggests a correlation between intracellular trafficking and severity of Menkes disease. [electronic resource] by Skjørringe, Tina Amstrup Pedersen, Per Salling Thorborg, Sidsel Nissen, Poul Gourdon, Pontus Birk Møller, Lisbeth Producer: 20180830 In: Scientific reports vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Levodopa-responsive infantile parkinsonism due to a novel mutation in the tyrosine hydroxylase gene and exacerbation by viral infections. [electronic resource] by Diepold, Katharina Schütz, Barbara Rostasy, Kevin Wilken, Bernd Hougaard, Pia Güttler, Flemming Romstad, Anne Birk Møller, Lisbeth Producer: 20050729 In: Movement disorders : official journal of the Movement Disorder Society vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Progressive cerebellar degenerative changes in the severe mental retardation syndrome caused by duplication of MECP2 and adjacent loci on Xq28. [electronic resource] by Reardon, William Donoghue, Veronica Murphy, Anne-Marie King, Mary D Mayne, Philip D Horn, Nina Birk Møller, Lisbeth Producer: 20110316 In: European journal of pediatrics vol. 169 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Low proportion of whole exon deletions causing phenylketonuria in Denmark and Germany. [electronic resource] by Birk Møller, Lisbeth Nygren, Anders O H Scott, Patrick Hougaard, Pia Bieber Nielsen, Jytte Hartmann, Caroline Güttler, Flemming Tyfield, Linda Zschocke, Johannes Producer: 20070228 In: Human mutation vol. 28 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)