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Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1families

✍ Scribed by Winbo, Annika; Stattin, Eva-Lena; Nordin, Charlotte; Diamant, Ulla-Britt; Persson, Johan; Jensen, Steen M; Rydberg, Annika


Book ID
125397711
Publisher
BioMed Central
Year
2014
Tongue
English
Weight
469 KB
Volume
14
Category
Article
ISSN
1471-2261

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