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SPECTRUM AND PREVALENCE OF CARDIAC RYANODINE RECEPTOR (RYR2) AND KIR2.1 (KCNJ2) MUTATIONS IN PATIENTS REFERRED FOR FAMILION® CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA (CPVT) GENETIC TESTING

✍ Scribed by Thomas E. Callis; Janet L. Carr; Lisa Susswein; Guido D. Pollevick; Michael Ackerman; Benjamin S. Salisbury


Book ID
118582532
Publisher
Elsevier Science
Year
2012
Tongue
English
Weight
91 KB
Volume
59
Category
Article
ISSN
1558-3597

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