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Next-generation sequencing (NGS) as a fast molecular diagnosis tool for left ventricular noncompaction in an infant with compound mutations in the MYBPC3 gene

✍ Scribed by Schaefer, Elise; Helms, Pauline; Marcellin, Luc; Desprez, Philippe; Billaud, Philippe; Chanavat, Valérie; Rousson, Robert; Millat, Gilles


Book ID
121773553
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
859 KB
Volume
57
Category
Article
ISSN
1769-7212

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