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Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death.

• Authors : Neubauer, Jacqueline¹ (AUTHOR) ; Wang, Zizun² (AUTHOR); Rougier, Jean-Sébastien² (AUTHOR)

Subjects: *LONG QT syndrome; *CARDIAC arrest; *AUTOPSY

• Source: International Journal of Legal Medicine. Nov2019, Vol. 133 Issue 6, p1733-1742. 10p.

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Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs

• Authors : Jeanett Edelmann; M Nastainczyk-Wulf; Tadeusz Dobosz

Subjects: ERG1 Potassium Channel; Heterozygote; congenital, hereditary, and neonatal diseases and abnormalities

• Source: International Journal of Legal Medicine. 131:333-338

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Long QT syndrome mutation detection by SNaPshot technique.

• Authors : Edelmann, Jeanett¹ ; Schumann, Stefanie²; Nastainczyk, Marina¹

Subjects: *LONG QT syndrome; *SINGLE nucleotide polymorphisms; *GENETIC mutation

• Source: International Journal of Legal Medicine. Nov2012, Vol. 126 Issue 6, p969-973. 5p.

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Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases

• Authors : Catarina Allegue; Angel Carracedo; Rocio Gil

Subjects: Adult; Male; ERG1 Potassium Channel

• Source: International Journal of Legal Medicine. 125:565-572

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Mutation analysis for the detection of long QT-syndrome (LQTS) associated SNPs.

• Authors : J., Edelmann¹ ; T., Dobosz²; M., Sobieszczanska³

Subjects: *GENETIC mutation; *CONGENITAL heart disease; *SINGLE nucleotide polymorphisms

• Source: International Journal of Legal Medicine. Mar2017, Vol. 131 Issue 2, p333-338. 6p.

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Long QT syndrome mutation detection by SNaPshot technique

• Authors : Daniela Husser-Bollmann; Stefanie Schumann; Jeanett Edelmann

Subjects: congenital, hereditary, and neonatal diseases and abnormalities; ERG1 Potassium Channel; Long QT syndrome

• Source: International journal of legal medicine. 126(6)

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Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in water

• Authors : Antti Levo; Päivi Laitinen; Heidi Fodstad

Subjects: Adult; Male; congenital, hereditary, and neonatal diseases and abnormalities

• Source: International Journal of Legal Medicine. 117:115-117

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Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study

• Authors : Wilhelm Haverkamp; Eric Schulze-Bahr; Birgit Engeland

Subjects: Male; Long QT syndrome; Population

• Source: International journal of legal medicine. 120(3)

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Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study

• Authors : Wedekind, Horst; Bajanowski, Thomas; Friederich, Patrick

• Source: International Journal of Legal Medicine; May 2006, Vol. 120 Issue: 3 p129-137, 9p

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Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases.

• Authors : Allegue, Catarina^1,2; Gil, Rocio^1,2; Blanco-Verea, Alejandro^1,2

Subjects: *CARDIOMYOPATHIES; *HUMAN chromosome abnormality diagnosis; *CARDIAC hypertrophy

• Source: International Journal of Legal Medicine. Jul2011, Vol. 125 Issue 4, p565-572. 8p.

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