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	1.	ATP-binding cassette subfamily A, member 4 intronic variants c.4773+3A>G and c.5461-10T>C cause Stargardt disease due to defective splicing. [electronic resource] by Jonsson, Frida Westin, Ida Maria Österman, Lennart Sandgren, Ola Burstedt, Marie Holmberg, Monica Golovleva, Irina Producer: 20181211 In: Acta ophthalmologica vol. 96 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis. [electronic resource] by Winbo, Annika Stattin, Eva-Lena Westin, Ida Maria Norberg, Anna Persson, Johan Jensen, Steen M Rydberg, Annika Producer: 20170724 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Genetic screening in sudden cardiac death in the young can save future lives. [electronic resource] by Stattin, Eva-Lena Westin, Ida Maria Cederquist, Kristina Jonasson, Jenni Jonsson, Björn-Anders Mörner, Stellan Norberg, Anna Krantz, Peter Wisten, Aase Producer: 20161012 In: International journal of legal medicine vol. 130 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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