Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice.

Autoria(s): Fokstuen S.; Munoz A.; Melacini P.; Iliceto S.; Perrot A.; Ozcelik C.; Jeanrenaud X.; Rieubland C.; Farr M.; Faber L.; Sigwart U.; Mach F.; Lerch R.; Antonarakis S.E.; Blouin J.L.
Data(s)

2011
Identificador

http://serval.unil.ch/?id=serval:BIB_6D6A127A886D

isbn:1468-6244 (Electronic)

pmid:21239446

doi:10.1136/jmg.2010.083345

isiid:000292958800013
Idioma(s)

en
Fonte

Journal of Medical Genetics, vol. 48, no. 8, pp. 572-576
Tipo

info:eu-repo/semantics/article

article
Acesso ao item digital