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	1.	Two novel mutations and coexistence of the 991C>T and the 1339C>T mutation on a single allele in the coproporphyrinogen oxidase gene in Swedish patients with hereditary coproporphyria. [electronic resource] by Wiman, Asa Floderus, Ylva Harper, Pauline Producer: 20021009 In: Journal of human genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Novel mutations and phenotypic effect of the splice site modulator IVS3-48C in nine Swedish families with erythropoietic protoporphyria. [electronic resource] by Wiman, Asa Floderus, Ylva Harper, Pauline Producer: 20030326 In: Journal of human genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Partial protoporphyrinogen oxidase (PPOX) gene deletions, due to different Alu-mediated mechanisms, identified by MLPA analysis in patients with variegate porphyria. [electronic resource] by Barbaro, Michela Kotajärvi, Maire Harper, Pauline Floderus, Ylva Producer: 20130723 In: Orphanet journal of rare diseases vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The prevalence of hepatitis C in patients with porphyria cutanea tarda in Stockholm, Sweden. [electronic resource] by Linde, Ylva Harper, Pauline Floderus, Ylva Ros, Anne-Marie Producer: 20050721 In: Acta dermato-venereologica vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Plasma porphobilinogen as a sensitive biomarker to monitor the clinical and therapeutic course of acute intermittent porphyria attacks. [electronic resource] by Sardh, Eliane Harper, Pauline Andersson, Dan E H Floderus, Ylva Producer: 20090618 In: European journal of internal medicine vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Haplotype analysis of Norwegian and Swedish patients with acute intermittent porphyria (AIP): Extreme haplotype heterogeneity for the mutation R116W. [electronic resource] by Tjensvoll, Kjersti Bruland, Ove Floderus, Ylva Skadberg, Øyvind Sandberg, Sverre Apold, Jaran Producer: 20040217 In: Disease markers vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Variations in porphobilinogen and 5-aminolevulinic acid concentrations in plasma and urine from asymptomatic carriers of the acute intermittent porphyria gene with increased porphyrin precursor excretion. [electronic resource] by Floderus, Ylva Sardh, Eliane Möller, Christer Andersson, Claes Rejkjaer, Lillan Andersson, Dan E H Harper, Pauline Producer: 20060502 In: Clinical chemistry vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A recurrent mutation in variegate porphyria patients from Chile and Sweden: Evidence for a common genetic background? [electronic resource] by van Serooskerken, Anne Moniek van Tuyll Ernst, Manon Bladergroen, Reno S Wolff, Carlos Floderus, Ylva Harper, Pauline Poblete-Gutiérrez, Pamela van Geel, Michel Frank, Jorge Producer: 20110421 In: Journal of dermatological science vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	International Porphyria Molecular Diagnostic Collaborative: an evidence-based database of verified pathogenic and benign variants for the porphyrias. [electronic resource] by Chen, Brenden Whatley, Sharon Badminton, Michael Aarsand, Aasne K Anderson, Karl E Bissell, D Montgomery Bonkovsky, Herbert L Cappellini, Maria D Floderus, Ylva Friesema, Edith C H Gouya, Laurent Harper, Pauline Kauppinen, Raili Loskove, Yonina Martásek, Pavel Phillips, John D Puy, Hervé Sandberg, Sverre Schmitt, Caroline To-Figueras, Jordi Weiss, Yedidyah Yasuda, Makiko Deybach, Jean-Charles Desnick, Robert J Producer: 20200427 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)