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Whole exome sequencing of familial hypercholesterolaemia patients negative for LDLR/APOB/PCSK9 mutations

✍ Scribed by Futema, M.; Plagnol, V.; Li, K.; Whittall, R. A.; Neil, H. A. W.; Seed, M.; Bertolini, S.; Calandra, S.; Descamps, O. S.; Graham, C. A.; Hegele, R. A.; Karpe, F.; Durst, R.; Leitersdorf, E.; Lench, N.; Nair, D. R.; Soran, H.; Van Bockxmeer, F. M.; Humphries, S. E.

Book ID: 125534082
Publisher: BMJ Publishing Group
Year: 2014
Tongue: English
Weight: 528 KB
Volume: 51
Category: Article
ISSN: 0022-2593
DOI: 10.1136/jmedgenet-2014-102405

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