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Evaluation of a new NGS method based on a custom AmpliSeq library and Ion Torrent PGM sequencing for the fast detection of genetic variations in cardiomyopathies

✍ Scribed by Millat, Gilles; Chanavat, Valérie; Rousson, Robert


Book ID
121823740
Publisher
Elsevier Science
Year
2014
Tongue
English
Weight
370 KB
Volume
433
Category
Article
ISSN
0009-8981

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