Publications

Author

Title

Year sorteringsordning

Fulltext

Winbo, Annika
Stattin, Eva-Lena
Westin, Ida Maria; et al.

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
BMC Medical Genetics, 18

2017

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Stattin, Eva-Lena
Westin, Ida Maria
Cederquist, Kristina; et al.

Genetic screening in sudden cardiac death in the young can save future lives
International journal of legal medicine (Print), 130(1): 59-66

2016

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Wisten, Aase
Boström, Ida Maria
Mörner, Stellan; et al.

Mutation analysis of cases of sudden unexplained death, 15 years after death: Prompt genetic evaluation after resuscitation can save future lives
Resuscitation, 83(10): 1229-1234

2012

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Stattin, Eva-Lena
Boström, Ida Maria
Winbo, Annika; et al.

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
BMC Cardiovascular Disorders, 12: 95-

2012

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