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Author/Creator Muggenthaler, Martina

1. 163 Genetic Modifiers in Carriers of the SCN5A E1784K Mutation with Variable Phenotypic Expression - Long QT3 / Brugada Syndrome Overlap Disease. (31st May 2014)

Authors:
Dullewe Wijeyeratne, Yanushi; Muggenthaler, Martina; Tanck, Michael W; Schott, Jean-Jacques; Kyndt, Florence; Probst, Vincent; Borggrefe, Martin; McKeown, Pascal; Veltmann, Christian; Crotti, Lia; Schwartz, Peter; Sharma, Sanjay; Makita, Naomasa; Roden, Dan; Behr, Elijah R
Journal:
Heart
Issue:
Volume 100:(2014)Supplement 3
Page Start:
A94
Record Type:
Journal Article
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4. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families. (December 2020)

Authors:
Wijeyeratne, Yanushi D.; Tanck, Michael W.; Mizusawa, Yuka; Batchvarov, Velislav; Barc, Julien; Crotti, Lia; Bos, J. Martijn; Tester, David J.; Muir, Alison; Veltmann, Christian; Ohno, Seiko; Page, Stephen P.; Galvin, Joseph; Tadros, Rafik; Muggenthaler, Martina; Raju, Hariharan; Denjoy, Isabelle...
Journal:
Circulation
Issue:
Volume 13:Number 6(2020)
Page Start:
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗